{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,31]],"date-time":"2026-10-31T01:21:05Z","timestamp":1793409665440,"version":"4.5.0"},"reference-count":49,"publisher":"Elsevier BV","issue":"9","license":[{"start":{"date-parts":[[2024,9,1]],"date-time":"2024-09-01T00:00:00Z","timestamp":1725148800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,9,1]],"date-time":"2024-09-01T00:00:00Z","timestamp":1725148800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["jaci-inpractice.org","clinicalkey.fr","clinicalkey.jp","clinicalkey.com.au","clinicalkey.es","clinicalkey.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["The Journal of Allergy and Clinical Immunology: In Practice"],"published-print":{"date-parts":[[2024,9]]},"DOI":"10.1016\/j.jaip.2024.06.046","type":"journal-article","created":{"date-parts":[[2024,7,10]],"date-time":"2024-07-10T18:33:20Z","timestamp":1720636400000},"page":"2490-2502.e6","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":9,"title":["MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort"],"prefix":"10.1016","volume":"12","author":[{"given":"Zeynep","family":"Gulec Koksal","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sevgi","family":"Bilgic Eltan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ezgi","family":"Topyildiz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ahmet","family":"Sezer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sevgi","family":"Keles","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Figen","family":"Celebi Celik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aylin","family":"Ozhan Kont","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Betul","family":"Gemici Karaaslan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Asena Pinar","family":"Sefer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zuhal","family":"Karali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elif","family":"Arik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Esra","family":"Ozek Yucel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Omer","family":"Akcal","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Leman Tuba","family":"Karakurt","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melek","family":"Yorgun Altunbas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Koray","family":"Yalcin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vedat","family":"Uygun","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gulcihan","family":"Ozek","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Royala","family":"Babayeva","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cigdem","family":"Aydogmus","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dilek","family":"Ozcan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ozlem","family":"Cavkaytar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ozlem","family":"Keskin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sara Sebnem","family":"Kilic","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ayca","family":"Kiykim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tugba","family":"Arikoglu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ferah","family":"Genel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nesrin","family":"Gulez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sukru Nail","family":"Guner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neslihan Edeer","family":"Karaca","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ismail","family":"Reisli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Necil","family":"Kutukculer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Derya Ufuk","family":"Altintas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ahmet","family":"Ozen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elif","family":"Karakoc Aydiner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Safa","family":"Baris","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jaip.2024.06.046_bib1","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1016\/j.jaci.2014.06.001","article-title":"MHC class I and II deficiencies","volume":"134","author":"Hanna","year":"2014","journal-title":"J\u00a0Allergy Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib2","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1016\/S0268-960X(96)90008-9","article-title":"Major histocompatibility complex class II deficiency: a clinical review","volume":"10","author":"Elhasid","year":"1996","journal-title":"Blood Rev"},{"key":"10.1016\/j.jaip.2024.06.046_bib3","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1146\/annurev.immunol.19.1.331","article-title":"The bare lymphocyte syndrome and the regulation of MHC expression","volume":"19","author":"Reith","year":"2001","journal-title":"Annu Rev Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib4","doi-asserted-by":"crossref","first-page":"140","DOI":"10.1016\/0090-1229(89)90121-9","article-title":"Combined immunodeficiency with abnormal expression of MHC class II genes","volume":"50","author":"Griscelli","year":"1989","journal-title":"Clin Immunol Immunopathol"},{"key":"10.1016\/j.jaip.2024.06.046_bib5","doi-asserted-by":"crossref","first-page":"5108","DOI":"10.1182\/blood-2011-05-352716","article-title":"Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients","volume":"118","author":"Ouederni","year":"2011","journal-title":"Blood"},{"key":"10.1016\/j.jaip.2024.06.046_bib6","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1146\/annurev.iy.12.040194.001355","article-title":"Assembly, transport, and function of MHC class II molecules","volume":"12","author":"Cresswell","year":"1994","journal-title":"Annu Rev Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib7","doi-asserted-by":"crossref","DOI":"10.3389\/fimmu.2021.669943","article-title":"Thymic epithelial cell alterations and defective thymopoiesis lead to central and peripheral tolerance perturbation in MHCII deficiency","volume":"12","author":"Ferrua","year":"2021","journal-title":"Front Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib8","doi-asserted-by":"crossref","first-page":"273","DOI":"10.1038\/3081","article-title":"A\u00a0gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients","volume":"20","author":"Masternak","year":"1998","journal-title":"Nat Genet"},{"key":"10.1016\/j.jaip.2024.06.046_bib9","doi-asserted-by":"crossref","first-page":"1045","DOI":"10.1093\/emboj\/16.5.1045","article-title":"RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency","volume":"16","author":"Durand","year":"1997","journal-title":"EMBO J"},{"key":"10.1016\/j.jaip.2024.06.046_bib10","doi-asserted-by":"crossref","first-page":"897","DOI":"10.1016\/S0092-8674(88)90389-3","article-title":"Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X","volume":"53","author":"Reith","year":"1988","journal-title":"Cell"},{"key":"10.1016\/j.jaip.2024.06.046_bib11","doi-asserted-by":"crossref","first-page":"135","DOI":"10.1016\/S0092-8674(05)80090-X","article-title":"Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)","volume":"75","author":"Steimle","year":"1993","journal-title":"Cell"},{"key":"10.1016\/j.jaip.2024.06.046_bib12","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1034\/j.1600-065X.2000.17813.x","article-title":"Lessons from the bare lymphocyte syndrome: molecular mechanisms regulating MHC class II expression","volume":"178","author":"Waldburger","year":"2000","journal-title":"Immunol Rev"},{"key":"10.1016\/j.jaip.2024.06.046_bib13","doi-asserted-by":"crossref","first-page":"1021","DOI":"10.1101\/gad.9.9.1021","article-title":"A\u00a0novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)","volume":"9","author":"Steimle","year":"1995","journal-title":"Genes Dev"},{"key":"10.1016\/j.jaip.2024.06.046_bib14","doi-asserted-by":"crossref","first-page":"954","DOI":"10.1182\/blood.2019002690","article-title":"Improved transplant survival and long-term disease outcome in children with MHC class II deficiency","volume":"135","author":"Lum","year":"2020","journal-title":"Blood"},{"key":"10.1016\/j.jaip.2024.06.046_bib15","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1007\/s00251-003-0609-2","article-title":"Splicing defect in RFXANK results in a moderate combined immunodeficiency and long-duration clinical course","volume":"55","author":"Prod'homme","year":"2003","journal-title":"Immunogenetics"},{"key":"10.1016\/j.jaip.2024.06.046_bib16","doi-asserted-by":"crossref","first-page":"1787","DOI":"10.4049\/jimmunol.167.3.1787","article-title":"Mutation in the class II trans-activator leading to a mild immunodeficiency","volume":"167","author":"Wiszniewski","year":"2001","journal-title":"J\u00a0Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib17","doi-asserted-by":"crossref","first-page":"1693","DOI":"10.1016\/j.jaci.2013.01.019","article-title":"Newborn screening for severe combined immunodeficiency does not identify bare lymphocyte syndrome","volume":"131","author":"Kuo","year":"2013","journal-title":"J\u00a0Allergy Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib18","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1007\/s12026-018-9019-2","article-title":"MHC II deficient infant identified by newborn screening program for SCID","volume":"66","author":"Marcus","year":"2018","journal-title":"Immunol Res"},{"key":"10.1016\/j.jaip.2024.06.046_bib19","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1016\/S0022-3476(05)80388-9","article-title":"Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome","volume":"123","author":"Klein","year":"1993","journal-title":"J\u00a0Pediatr"},{"key":"10.1016\/j.jaip.2024.06.046_bib20","doi-asserted-by":"crossref","first-page":"356","DOI":"10.1136\/adc.83.4.356","article-title":"Clinical course of patients with major histocompatibility complex class II deficiency","volume":"83","author":"Saleem","year":"2000","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.jaip.2024.06.046_bib21","doi-asserted-by":"crossref","first-page":"818","DOI":"10.1016\/j.bbmt.2010.01.002","article-title":"Allogeneic stem cell transplantation using myeloablative and reduced-intensity conditioning in patients with major histocompatibility complex class II deficiency","volume":"16","author":"Al-Mousa","year":"2010","journal-title":"Biol Blood Marrow Transplant"},{"key":"10.1016\/j.jaip.2024.06.046_bib22","doi-asserted-by":"crossref","first-page":"580","DOI":"10.1182\/blood.V85.2.580.580","article-title":"Bone marrow transplantation in major histocompatibility complex class II deficiency: a single-center study of 19 patients","volume":"85","author":"Klein","year":"1995","journal-title":"Blood"},{"key":"10.1016\/j.jaip.2024.06.046_bib23","doi-asserted-by":"crossref","first-page":"865","DOI":"10.1007\/s10875-013-9863-8","article-title":"Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients","volume":"33","author":"Ben-Mustapha","year":"2013","journal-title":"J\u00a0Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib24","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1186\/1710-1492-8-14","article-title":"Clinical, immunological and genetic features in eleven Algerian patients with major histocompatibility complex class II expression deficiency","volume":"8","author":"Djidjik","year":"2012","journal-title":"Allergy Asthma Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib25","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1016\/j.jaip.2018.07.046","article-title":"MHC-II deficiency among Egyptians: novel mutations and unique phenotypes","volume":"7","author":"El Hawary","year":"2019","journal-title":"J\u00a0Allergy Clin Immunol Pract"},{"key":"10.1016\/j.jaip.2024.06.046_bib26","doi-asserted-by":"crossref","first-page":"379","DOI":"10.1007\/s10875-008-9191-6","article-title":"Primary immunodeficiency disorders: survey of pediatricians in Kuwait","volume":"28","author":"Al-Herz","year":"2008","journal-title":"J\u00a0Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib27","doi-asserted-by":"crossref","DOI":"10.1093\/ofid\/ofaa314","article-title":"A\u00a0novel RFXANK mutation in a Chinese child with MHC II deficiency: case report and literature review","volume":"7","author":"Cai","year":"2020","journal-title":"Open Forum Infect Dis"},{"key":"10.1016\/j.jaip.2024.06.046_bib28","doi-asserted-by":"crossref","first-page":"1941","DOI":"10.1007\/s10875-023-01562-z","article-title":"Clinical, immunological, and genetic findings in Iranian patients with MHC-II deficiency: confirmation of c.162delG RFXANK founder mutation in the Iranian population","volume":"43","author":"Mousavi Khorshidi","year":"2023","journal-title":"J\u00a0Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib29","doi-asserted-by":"crossref","first-page":"747","DOI":"10.1007\/s00251-002-0521-1","article-title":"Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II","volume":"54","author":"Wiszniewski","year":"2003","journal-title":"Immunogenetics"},{"key":"10.1016\/j.jaip.2024.06.046_bib30","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1007\/s002510050619","article-title":"Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B","volume":"51","author":"Wiszniewski","year":"2000","journal-title":"Immunogenetics"},{"key":"10.1016\/j.jaip.2024.06.046_bib31","doi-asserted-by":"crossref","DOI":"10.1111\/sji.13335","article-title":"A\u00a0large single-center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey","volume":"99","author":"Unsal","year":"2024","journal-title":"Scand J Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib32","doi-asserted-by":"crossref","first-page":"158","DOI":"10.1016\/j.jaip.2022.10.003","article-title":"The Middle East and North Africa diagnosis and management guidelines for inborn errors of immunity","volume":"11","author":"Baris","year":"2023","journal-title":"J\u00a0Allergy Clin Immunol Pract"},{"key":"10.1016\/j.jaip.2024.06.046_bib33","doi-asserted-by":"crossref","first-page":"1473","DOI":"10.1007\/s10875-022-01289-3","article-title":"Human inborn errors of immunity: 2022 update on the classification from the International Union of Immunological Societies Expert Committee","volume":"42","author":"Tangye","year":"2022","journal-title":"J\u00a0Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib34","doi-asserted-by":"crossref","first-page":"2790","DOI":"10.1016\/j.jaip.2019.06.011","article-title":"Abatacept as a long-term targeted therapy for LRBA deficiency","volume":"7","author":"Kiykim","year":"2019","journal-title":"J\u00a0Allergy Clin Immunol Pract"},{"key":"10.1016\/j.jaip.2024.06.046_bib35","doi-asserted-by":"crossref","first-page":"3108","DOI":"10.1111\/all.15331","article-title":"Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency","volume":"77","author":"Catak","year":"2022","journal-title":"Allergy"},{"key":"10.1016\/j.jaip.2024.06.046_bib36","doi-asserted-by":"crossref","first-page":"1634","DOI":"10.1016\/j.jaci.2023.08.004","article-title":"Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency","volume":"152","author":"Taghizade","year":"2023","journal-title":"J\u00a0Allergy Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib37","doi-asserted-by":"crossref","DOI":"10.1016\/j.clim.2023.109757","article-title":"Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients","volume":"255","author":"Yakici","year":"2023","journal-title":"Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib38","doi-asserted-by":"crossref","first-page":"1814","DOI":"10.3906\/sag-2010-176","article-title":"Reference values for T and B lymphocyte subpopulations in Turkish children and adults","volume":"51","author":"Besci","year":"2021","journal-title":"Turk J Med Sci"},{"key":"10.1016\/j.jaip.2024.06.046_bib39","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1007\/s10875-021-01191-4","article-title":"Expanding the clinical and immunological phenotypes and natural history of MALT1 deficiency","volume":"42","author":"Sefer","year":"2022","journal-title":"J\u00a0Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib40","doi-asserted-by":"crossref","first-page":"1004","DOI":"10.1111\/all.15010","article-title":"Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency","volume":"77","author":"Kolukisa","year":"2022","journal-title":"Allergy"},{"key":"10.1016\/j.jaip.2024.06.046_bib41","doi-asserted-by":"crossref","DOI":"10.1016\/j.clim.2023.109696","article-title":"Epidemiology of combined immunodeficiencies affecting cellular and humoral immunity- a multicentric retrospective cohort study from the Arabian Peninsula","volume":"254","author":"Al-Herz","year":"2023","journal-title":"Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib42","doi-asserted-by":"crossref","first-page":"1036","DOI":"10.1007\/s10875-022-01262-0","article-title":"Clinical and laboratory factors affecting the prognosis of severe combined immunodeficiency","volume":"42","author":"Ozturk","year":"2022","journal-title":"J\u00a0Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib43","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1016\/j.clim.2019.04.012","article-title":"Persisting enteropathy and disturbed adaptive mucosal\u00a0immunity due to MHC class II deficiency","volume":"203","author":"Posovszky","year":"2019","journal-title":"Clin Immunol"},{"key":"10.1016\/j.jaip.2024.06.046_bib44","doi-asserted-by":"crossref","DOI":"10.1016\/j.waojou.2022.100657","article-title":"Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: a worldwide study","volume":"15","author":"El-Sayed","year":"2022","journal-title":"World Allergy Organ J"},{"key":"10.1016\/j.jaip.2024.06.046_bib45","doi-asserted-by":"crossref","first-page":"1583","DOI":"10.1084\/jem.20062287","article-title":"CD40 ligand and MHC class II expression are essential for human peripheral B cell tolerance","volume":"204","author":"Herve","year":"2007","journal-title":"J\u00a0Exp Med"},{"key":"10.1016\/j.jaip.2024.06.046_bib46","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1016\/S0140-6736(03)12513-5","article-title":"Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968-99","volume":"361","author":"Antoine","year":"2003","journal-title":"Lancet"},{"key":"10.1016\/j.jaip.2024.06.046_bib47","doi-asserted-by":"crossref","first-page":"817","DOI":"10.1038\/bmt.2008.399","article-title":"Unrelated cord blood transplantation and reduced-intensity conditioning regimen for graft failure in a child with major histocompatibility complex class II deficiency","volume":"43","author":"Bonduel","year":"2009","journal-title":"Bone Marrow Transplant"},{"key":"10.1016\/j.jaip.2024.06.046_bib48","doi-asserted-by":"crossref","first-page":"510","DOI":"10.1111\/j.1365-2141.2006.06213.x","volume":"134","author":"Renella","year":"2006","journal-title":"Br J Haematol"},{"key":"10.1016\/j.jaip.2024.06.046_bib49","doi-asserted-by":"crossref","first-page":"E80","DOI":"10.1111\/j.1399-3046.2010.01292.x","article-title":"MHC class II deficiency cured by unrelated mismatched umbilical cord blood transplantation: case report and review of 68 cases in the literature","volume":"15","author":"Siepermann","year":"2011","journal-title":"Pediatr Transplant"}],"container-title":["The Journal of Allergy and Clinical Immunology: In Practice"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2213219824006883?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2213219824006883?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,11,2]],"date-time":"2024-11-02T08:28:59Z","timestamp":1730536139000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2213219824006883"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,9]]},"references-count":49,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2024,9]]}},"alternative-id":["S2213219824006883"],"URL":"https:\/\/doi.org\/10.1016\/j.jaip.2024.06.046","relation":{},"ISSN":["2213-2198"],"issn-type":[{"value":"2213-2198","type":"print"}],"subject":[],"published":{"date-parts":[[2024,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort","name":"articletitle","label":"Article Title"},{"value":"The Journal of Allergy and Clinical Immunology: In Practice","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaip.2024.06.046","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 American Academy of Allergy, Asthma & Immunology","name":"copyright","label":"Copyright"}]}}