{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,10]],"date-time":"2026-04-10T17:24:01Z","timestamp":1775841841063,"version":"3.50.1"},"reference-count":9,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2022,7,12]],"date-time":"2022-07-12T00:00:00Z","timestamp":1657584000000},"content-version":"am","delay-in-days":284,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2021,10,1]],"date-time":"2021-10-01T00:00:00Z","timestamp":1633046400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/100010661","name":"Horizon 2020 Framework Programme","doi-asserted-by":"publisher","award":["643578"],"award-info":[{"award-number":["643578"]}],"id":[{"id":"10.13039\/100010661","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001665","name":"French National Research Agency","doi-asserted-by":"publisher","award":["ANR-11-INBS-0010"],"award-info":[{"award-number":["ANR-11-INBS-0010"]}],"id":[{"id":"10.13039\/501100001665","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100006489","name":"Commissariat \u00e0 l'\u00c9nergie Atomique et aux \u00c9nergies Alternatives","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100006489","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinica Chimica Acta"],"published-print":{"date-parts":[[2021,10]]},"DOI":"10.1016\/j.cca.2021.07.005","type":"journal-article","created":{"date-parts":[[2021,7,8]],"date-time":"2021-07-08T05:34:11Z","timestamp":1625722451000},"page":"104-106","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":9,"special_numbering":"C","title":["SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy"],"prefix":"10.1016","volume":"521","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2651-650X","authenticated-orcid":false,"given":"Alexandre","family":"Raynor","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0013-9857","authenticated-orcid":false,"given":"Walid","family":"Haouari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bobby G.","family":"Ng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sophie","family":"Cholet","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Annie","family":"Harroche","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Celia","family":"Raulet-Bussian","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Samra","family":"Lounis-Ouaras","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sandrine","family":"Vuillaumier-Barrot","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tiffany","family":"Pascreau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8847-8935","authenticated-orcid":false,"given":"Delphine","family":"Borgel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hudson H.","family":"Freeze","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6787-4149","authenticated-orcid":false,"given":"Fran\u00e7ois","family":"Fenaille","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8411-3309","authenticated-orcid":false,"given":"Arnaud","family":"Bruneel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.cca.2021.07.005_b0005","article-title":"SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation","volume":"25","author":"Marquardt","year":"2020","journal-title":"Mol. Genet. Metab. Rep."},{"issue":"1","key":"10.1016\/j.cca.2021.07.005_b0010","first-page":"122","article-title":"SLC37A4-CDG: Second patient","volume":"58","author":"Wilson","year":"2021","journal-title":"JIMD Rep."},{"issue":"21","key":"10.1016\/j.cca.2021.07.005_b0015","first-page":"00144","article-title":"A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction","volume":"S0002\u20139297","author":"Ng","year":"2021","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.cca.2021.07.005_b0020","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1016\/j.cca.2017.04.022","article-title":"Two-dimensional electrophoresis highlights haptoglobin beta chain as an additional biomarker of congenital disorders of glycosylation","volume":"470","author":"Bruneel","year":"2017","journal-title":"Clin. Chim. Acta"},{"key":"10.1016\/j.cca.2021.07.005_b0025","article-title":"MAN1B1-CDG: three new individuals and associated biochemical profiles","volume":"28","author":"Sakhi","year":"2021","journal-title":"Mol. Genet. Metab. Rep."},{"issue":"24","key":"10.1016\/j.cca.2021.07.005_b0030","doi-asserted-by":"crossref","first-page":"3123","DOI":"10.1002\/elps.201800021","article-title":"Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation","volume":"39","author":"Bruneel","year":"2018","journal-title":"Electrophoresis"},{"issue":"10","key":"10.1016\/j.cca.2021.07.005_b0035","doi-asserted-by":"crossref","DOI":"10.1016\/j.bbagen.2020.129652","article-title":"CDG biochemical screening: Where do we stand?","volume":"1864","author":"Bruneel","year":"2020","journal-title":"Biochim. Biophys. Acta, Gen. Subj."},{"issue":"24","key":"10.1016\/j.cca.2021.07.005_b0040","doi-asserted-by":"crossref","first-page":"3133","DOI":"10.1002\/elps.201800020","article-title":"Use of Endoglycosidase H as a diagnostic tool for MAN1B1-CDG patients","volume":"39","author":"Duvet","year":"2018","journal-title":"Electrophoresis"},{"issue":"6","key":"10.1016\/j.cca.2021.07.005_b0045","doi-asserted-by":"crossref","first-page":"1349","DOI":"10.1002\/jimd.12291","article-title":"Serum bikunin isoforms in congenital disorders of glycosylation and linkeropathies","volume":"43","author":"Haouari","year":"2020","journal-title":"J. Inherit. Metab. Dis."}],"container-title":["Clinica Chimica Acta"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0009898121002369?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0009898121002369?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,2]],"date-time":"2025-11-02T20:04:14Z","timestamp":1762113854000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0009898121002369"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,10]]},"references-count":9,"alternative-id":["S0009898121002369"],"URL":"https:\/\/doi.org\/10.1016\/j.cca.2021.07.005","relation":{},"ISSN":["0009-8981"],"issn-type":[{"value":"0009-8981","type":"print"}],"subject":[],"published":{"date-parts":[[2021,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy","name":"articletitle","label":"Article Title"},{"value":"Clinica Chimica Acta","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.cca.2021.07.005","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2021 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}