{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T23:01:37Z","timestamp":1775084497819,"version":"3.50.1"},"reference-count":58,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2018,3,1]],"date-time":"2018-03-01T00:00:00Z","timestamp":1519862400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2018,3,1]],"date-time":"2018-03-01T00:00:00Z","timestamp":1519862400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.es","elsevier.es","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Actas Dermo-Sifiliogr\u00e1ficas"],"published-print":{"date-parts":[[2018,3]]},"DOI":"10.1016\/j.ad.2017.08.008","type":"journal-article","created":{"date-parts":[[2017,11,26]],"date-time":"2017-11-26T19:30:39Z","timestamp":1511724639000},"page":"104-122","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":16,"title":["Diagn\u00f3stico gen\u00e9tico de la epiderm\u00f3lisis bullosa: recomendaciones de un grupo espa\u00f1ol de expertos"],"prefix":"10.1016","volume":"109","author":[{"given":"C.","family":"S\u00e1nchez-Jimeno","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.J.","family":"Esc\u00e1mez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Ayuso","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.J.","family":"Trujillo-Tiebas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"del R\u00edo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ad.2017.08.008_bib0295","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1186\/1750-1172-5-12","article-title":"Inherited epidermolysis bullosa","volume":"28","author":"Fine","year":"2010","journal-title":"Orphanet J Rare Dis."},{"key":"10.1016\/j.ad.2017.08.008_bib0585","doi-asserted-by":"crossref","first-page":"1103","DOI":"10.1016\/j.jaad.2014.01.903","article-title":"Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification","volume":"70","author":"Fine","year":"2014","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0305","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1016\/j.jaad.2012.01.045","article-title":"Squamous cell carcinoma and junctional epidermolysis bullosa","volume":"66","author":"Fine","year":"2012","journal-title":"J Am Acad Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0590","article-title":"Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa - best clinical practice guidelines","author":"Mellerio","year":"2015","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0315","series-title":"Gu\u00eda de atenci\u00f3n cl\u00ednica integral de la epiderm\u00f3lisis bullosa hereditaria","author":"Baquero-Fern\u00e1ndez","year":"2008"},{"key":"10.1016\/j.ad.2017.08.008_bib0320","doi-asserted-by":"crossref","first-page":"890","DOI":"10.1016\/j.ad.2013.03.006","article-title":"Prevalence of dystrophic epidermolysis bullosa in Spain: A population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care","volume":"104","author":"Hernandez-Mart\u00edn","year":"2013","journal-title":"Actas Dermosifiliogr."},{"key":"10.1016\/j.ad.2017.08.008_bib0325","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1186\/1750-1172-9-76","article-title":"Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa","volume":"9","author":"El Hachem","year":"2014","journal-title":"Orphanet J Rare Dis."},{"key":"10.1016\/j.ad.2017.08.008_bib0330","doi-asserted-by":"crossref","first-page":"376","DOI":"10.1016\/j.ad.2015.01.007","article-title":"Innovative therapeutic strategies for recessive dystrophic epidermolysis bullosa","volume":"106","author":"Larcher","year":"2015","journal-title":"Actas Dermosifiliogr."},{"key":"10.1016\/j.ad.2017.08.008_bib0595","doi-asserted-by":"crossref","first-page":"6","DOI":"10.5582\/irdr.2017.01005","article-title":"Novel and emerging therapies in the treatment of recessive dystrophic epidermolysis bullosa","volume":"6","author":"Rashidghamat","year":"2017","journal-title":"Intractable Rare Dis Res."},{"key":"10.1016\/j.ad.2017.08.008_bib0340","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1111\/exd.12084","article-title":"One goal, different strategies--molecular and cellular approaches for the treatment of inherited skin fragility disorders","volume":"22","author":"H\u00fcnefeld","year":"2013","journal-title":"Exp Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0600","doi-asserted-by":"crossref","unstructured":"Lwin, SM, McGrath, JA. Gene Therapy for Inherited Skin Disorders. In: eLS. John Wiley & Sons, Ltd: Chichester. 2017.","DOI":"10.1002\/9780470015902.a0026940"},{"key":"10.1016\/j.ad.2017.08.008_bib0350","doi-asserted-by":"crossref","first-page":"1719","DOI":"10.1038\/jid.2013.137","article-title":"Systemic protein therapy for recessive dystrophic epidermolysis bullosa: How far are we from clinical translation?","volume":"133","author":"Hovnanian","year":"2013","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0605","doi-asserted-by":"crossref","first-page":"1211","DOI":"10.1016\/j.jid.2017.02.011","article-title":"The \u201cKelch\u201d surprise: KLHL24, a new player in the pathogenesis of skin fragility","volume":"137","author":"Has","year":"2017","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0360","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1146\/annurev-genom-090413-025540","article-title":"The genetics of skin fragility","volume":"15","author":"Has","year":"2014","journal-title":"Annu Rev Genomics Hum Genet."},{"key":"10.1016\/j.ad.2017.08.008_bib0365","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1016\/j.matbio.2013.07.007","article-title":"Disorders of the cutaneous basement membrane zone--the paradigm of epidermolysis bullosa","volume":"33","author":"Bruckner-Tuderman","year":"2014","journal-title":"Matrix Biol."},{"key":"10.1016\/j.ad.2017.08.008_bib0370","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1111\/bjd.13190","article-title":"Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory","volume":"172","author":"Takeichi","year":"2015","journal-title":"Br J Dermatol."},{"issue":"11-12","key":"10.1016\/j.ad.2017.08.008_bib0375","first-page":"491","article-title":"Diagnosis of autoimmune bullous skin diseases","volume":"54","author":"Zillikens","year":"2008","journal-title":"Clin Lab."},{"key":"10.1016\/j.ad.2017.08.008_bib0380","first-page":"812029","article-title":"Clinical presentation, pathogenesis, diagnosis, and treatment of epidermolysis bullosa acquisita","author":"Ludwig","year":"2013","journal-title":"ISRN Dermatol"},{"key":"10.1016\/j.ad.2017.08.008_bib0385","doi-asserted-by":"crossref","first-page":"683","DOI":"10.1111\/j.1365-2133.2011.10428.x","article-title":"Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex","volume":"165","author":"Garc\u00eda","year":"2011","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0390","series-title":"Bases moleculares de la epiderm\u00f3lisis bullosa simple en Espa\u00f1a","author":"Santiago","year":"2017"},{"key":"10.1016\/j.ad.2017.08.008_bib0395","doi-asserted-by":"crossref","first-page":"e125","DOI":"10.1111\/j.1525-1470.2012.01748.x","article-title":"Epidermolysis bullosa simplex with mottled pigmentation: A family report and review","volume":"30","author":"Echeverr\u00eda-Garc\u00eda","year":"2013","journal-title":"Pediatr Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0400","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1111\/exd.12938","article-title":"Identification of 2rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia","volume":"25","author":"Menc\u00eda","year":"2016","journal-title":"Exp Dermatology."},{"key":"10.1016\/j.ad.2017.08.008_bib0405","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1111\/j.1365-2133.2010.09713.x","article-title":"The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation","volume":"163","author":"Escamez","year":"2010","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.ad.2017.08.008_bib0410","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1159\/000330331","article-title":"A recurrent nonsense mutation occurring as a de novo event in a patient with recessive dystrophic epidermolysis bullosa","volume":"223","author":"Cuadrado-Corrales","year":"2011","journal-title":"Dermatology."},{"key":"10.1016\/j.ad.2017.08.008_bib0415","doi-asserted-by":"crossref","first-page":"1204","DOI":"10.1002\/humu.21576","article-title":"Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history","volume":"32","author":"Has","year":"2011","journal-title":"Hum Mutat."},{"key":"10.1016\/j.ad.2017.08.008_bib0420","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1186\/s13023-014-0211-8","article-title":"Oxidative stress and mitochondrial dysfunction in Kindler syndrome","volume":"21","author":"Zapatero-Solana","year":"2014","journal-title":"Orphanet J Rare Dis."},{"key":"10.1016\/j.ad.2017.08.008_bib0425","unstructured":"Zapatero-Solana E. Estr\u00e9s oxidativo y disfunci\u00f3n mitocondrial en la patogenia del s\u00edndrome de Kindler. Madrid; Universidad Complutense de Madrid; 2015."},{"key":"10.1016\/j.ad.2017.08.008_bib0430","unstructured":"Aguirregoicoa E. S\u00edndrome de Kindler: identificaci\u00f3n de mutaciones y estudio de los hallazgos cl\u00ednicos, bioqu\u00edmicos y moleculares [tesis doctoral en curso]. Madrid; Universidad Complutense de Madrid"},{"key":"10.1016\/j.ad.2017.08.008_bib0435","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1016\/j.ad.2010.06.003","article-title":"Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa","volume":"101","author":"Cepeda-Vald\u00e9s","year":"2010","journal-title":"Actas Dermosifiliogr."},{"key":"10.1016\/j.ad.2017.08.008_bib0440","doi-asserted-by":"crossref","first-page":"692","DOI":"10.4103\/0378-6323.102358","article-title":"Immunofluorescence antigen mapping for hereditary epidermolysis bullosa","volume":"78","author":"Rao","year":"2012","journal-title":"Indian J Dermatol Venereol Leprol."},{"key":"10.1016\/j.ad.2017.08.008_bib0445","doi-asserted-by":"crossref","first-page":"1100","DOI":"10.1002\/humu.21551","article-title":"The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations","volume":"32","author":"Van den Akker","year":"2011","journal-title":"Hum Mutat."},{"key":"10.1016\/j.ad.2017.08.008_bib0450","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1002\/humu.20652","article-title":"The human intermediate filament database: Comprehensive information on a gene family involved in many human diseases","volume":"29","author":"Szeverenyi","year":"2008","journal-title":"Hum Mutat"},{"key":"10.1016\/j.ad.2017.08.008_bib0455","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1186\/1471-2350-11-139","article-title":"A prevalent mutation with founder effect in Spanish recessive dystrophic epidermolysis bullosa families","volume":"11","author":"Cuadrado-Corrales","year":"2010","journal-title":"BMC Med Genet"},{"key":"10.1016\/j.ad.2017.08.008_bib0460","series-title":"Epidermolisis bullosa distr\u00f3fica en poblaci\u00f3n espa\u00f1ola: efecto fundador y dataci\u00f3n de la mutaci\u00f3n c.6527insC en el gen COL7A1","author":"S\u00e1nchez-Jimeno","year":"2013"},{"key":"10.1016\/j.ad.2017.08.008_bib0465","doi-asserted-by":"crossref","first-page":"226","DOI":"10.1111\/j.1365-2133.2012.11128.x","article-title":"Recessive dystrophic epidermolysis bullosa: The origin of the c.6527insC mutation in the Spanish population","volume":"168","author":"Sanchez-Jimeno","year":"2012","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0470","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/j.jdermsci.2011.11.010","article-title":"Novel and recurrent COL7A1 mutations in Chilean patients with dystrophic epidermolysis bullosa","volume":"65","author":"Rodr\u00edguez","year":"2012","journal-title":"J Dermatol Sci."},{"key":"10.1016\/j.ad.2017.08.008_bib0475","doi-asserted-by":"crossref","first-page":"674","DOI":"10.1038\/gt.2011.12","article-title":"Risk assessment in skin gene therapy: Viral-cellular fusion transcripts generated by proviral transcriptional read-through in keratinocytes transduced with self-inactivating lentiviral vectors","volume":"18","author":"Almarza","year":"2011","journal-title":"Gene Ther."},{"key":"10.1016\/j.ad.2017.08.008_bib0480","doi-asserted-by":"crossref","first-page":"2186","DOI":"10.1038\/sj.mt.6300292","article-title":"Safe selection of genetically manipulated human primary keratinocytes with very high growth potential using CD24","volume":"15","author":"Bergoglio","year":"2007","journal-title":"Mol Ther."},{"key":"10.1016\/j.ad.2017.08.008_bib0485","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1111\/exd.12203","article-title":"Keratinocyte cell lines derived from severe generalized recessive epidermolysis bullosa patients carrying a highly recurrent COL7A1 homozygous mutation: Models to assess cell and gene therapies in vitro and in vivo","volume":"22","author":"Chamorro","year":"2013","journal-title":"Exp Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0490","doi-asserted-by":"crossref","first-page":"808","DOI":"10.1111\/bjd.12202","article-title":"Epidermolysis bullosa simplex with PLEC mutations: New phenotypes and new mutations","volume":"168","author":"Charlesworth","year":"2013","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0495","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1111\/bjd.12741","article-title":"Aplasia cutis congenita with dystrophic epidermolysis bullosa: Clinical and mutational study","volume":"170","author":"Chiaverini","year":"2014","journal-title":"Br J Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0500","doi-asserted-by":"crossref","first-page":"1977","DOI":"10.1038\/mt.2008.204","article-title":"Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted lentiviral vectors","volume":"16","author":"Di Nunzio","year":"2008","journal-title":"Mol Ther."},{"key":"10.1016\/j.ad.2017.08.008_bib0505","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1089\/hum.2004.15.921","article-title":"Construction of skin equivalents for gene therapy of recessive dystrophic epidermolysis bullosa","volume":"15","author":"Gache","year":"2004","journal-title":"Hum Gene Ther."},{"key":"10.1016\/j.ad.2017.08.008_bib0510","doi-asserted-by":"crossref","first-page":"571","DOI":"10.1038\/jid.2013.308","article-title":"Long-term survival of type XVII collagen revertant cells in an animal model of revertant cell therapy","volume":"134","author":"Gosty\u0144ski","year":"2014","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0515","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1111\/exd.12304","article-title":"Pigmentation and melanocyte supply to the epidermis depend on type XVII collagen","volume":"23","author":"Gosty\u0144ski","year":"2014","journal-title":"Exp Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0520","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1159\/000313507","article-title":"X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient","volume":"221","author":"Hern\u00e1ndez-Mart\u00edn","year":"2010","journal-title":"Dermatology."},{"key":"10.1016\/j.ad.2017.08.008_bib0525","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1016\/j.ad.2012.12.006","article-title":"Reference centers for epidermolysis bullosa and ichthyosis: An urgent need in Spain","volume":"104","author":"Hern\u00e1ndez-Martin","year":"2013","journal-title":"Actas Dermosifiliogr."},{"key":"10.1016\/j.ad.2017.08.008_bib0530","doi-asserted-by":"crossref","first-page":"2097","DOI":"10.1038\/jid.2014.118","article-title":"Mechanisms of natural gene therapy in dystrophic epidermolysis bullosa","volume":"134","author":"Kiritsi","year":"2014","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0535","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1016\/j.ad.2011.03.006","article-title":"Skin bioengineering: Preclinical and clinical applications","volume":"103","author":"Mart\u00ednez-Santamar\u00eda","year":"2012","journal-title":"Actas Dermosifiliogr."},{"key":"10.1016\/j.ad.2017.08.008_bib0540","doi-asserted-by":"crossref","first-page":"2407","DOI":"10.1038\/jid.2010.163","article-title":"Revertant mosaicism due to a second-site mutation in COL7A1 in a patient with recessive dystrophic epidermolysis bullosa","volume":"130","author":"Pasmooij","year":"2010","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0545","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1016\/j.bbrc.2005.10.216","article-title":"Sustained phenotypic reversion of junctional epidermolysis bullosa dog keratinocytes: Establishment of an immunocompetent animal model for cutaneous gene therapy","volume":"339","author":"Spirito","year":"2006","journal-title":"Biochem Biophys Res Commun."},{"key":"10.1016\/j.ad.2017.08.008_bib0550","doi-asserted-by":"crossref","first-page":"239","DOI":"10.1111\/j.0022-202X.2005.23818.x","article-title":"Epidermolysis bullosa simplex: recurrent and de novo mutations in the KRT5 and KRT14 genes, phenotype\/genotype correlations, and implications for genetic counseling and prenatal diagnosis","volume":"125","author":"Pfendner","year":"2005","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0555","doi-asserted-by":"crossref","first-page":"239","DOI":"10.1016\/j.det.2009.12.004","article-title":"Genetic counseling in epidermolysis bullosa","volume":"28","author":"Sybert","year":"2010","journal-title":"Dermatol Clin."},{"key":"10.1016\/j.ad.2017.08.008_bib0560","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1016\/j.det.2010.02.001","article-title":"Prenatal diagnosis of epidermolysis bullosa","volume":"28","author":"Fassihi","year":"2010","journal-title":"Dermatol Clin."},{"key":"10.1016\/j.ad.2017.08.008_bib0565","doi-asserted-by":"crossref","first-page":"908","DOI":"10.1002\/pd.4137","article-title":"The key role of ultrasound examination in the prenatal diagnosis of epidermolysis bullosa with pyloric atresia","volume":"33","author":"Maurice","year":"2013","journal-title":"Prenat Diagn."},{"key":"10.1016\/j.ad.2017.08.008_bib0570","doi-asserted-by":"crossref","first-page":"2815","DOI":"10.1038\/jid.2008.143","article-title":"Immunofluorescence analysis of villous trophoblasts: A tool for prenatal diagnosis of inherited epidermolysis bullosa with pyloric atresia","volume":"128","author":"D\u2019Alessio","year":"2008","journal-title":"J Invest Dermatol."},{"key":"10.1016\/j.ad.2017.08.008_bib0575","doi-asserted-by":"crossref","first-page":"913","DOI":"10.3390\/jcm3030913","article-title":"Non-invasive prenatal diagnosis in the management of preimplantation genetic diagnosis pregnancies","volume":"14","author":"Bustamante-Aragones","year":"2014","journal-title":"J Clin Med."},{"key":"10.1016\/j.ad.2017.08.008_bib0580","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1093\/humrep\/dem327","article-title":"Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis","volume":"23","author":"Goossens","year":"2008","journal-title":"Hum Reprod."}],"container-title":["Actas Dermo-Sifiliogr\u00e1ficas"],"original-title":[],"language":"es","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0001731017305069?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0001731017305069?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,11]],"date-time":"2025-09-11T01:06:54Z","timestamp":1757552814000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0001731017305069"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,3]]},"references-count":58,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2018,3]]}},"alternative-id":["S0001731017305069"],"URL":"https:\/\/doi.org\/10.1016\/j.ad.2017.08.008","relation":{},"ISSN":["0001-7310"],"issn-type":[{"value":"0001-7310","type":"print"}],"subject":[],"published":{"date-parts":[[2018,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Diagn\u00f3stico gen\u00e9tico de la epiderm\u00f3lisis bullosa: recomendaciones de un grupo espa\u00f1ol de expertos","name":"articletitle","label":"Article Title"},{"value":"Actas Dermo-Sifiliogr\u00e1ficas","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ad.2017.08.008","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 AEDV. Published by Elsevier Espa\u00f1a, S.L.U. All rights reserved.","name":"copyright","label":"Copyright"}]}}