Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations-Reference-Cited by-同舟云学术

Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations

Published:2021-03 Issue:5 Volume:184 Page:960-962
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Hérissé A.L.¹,Charlesworth A.¹,Bellon N.²,Leclerc‐Mercier S.²,Bourrat E.³,Hadj‐Rabia S.²^ORCID,Bodemer C.²,Lacour J.P.¹,Chiaverini C.¹^ORCID

Affiliation:

1. Departments of Dermatology, Referral Center for GenodermatosesDepartment of Dermatology, Referral Center for Genodermatoses Centre Hospitalier Universitaire de Nice Nice

2. Department of Dermatology, Referral Center for Genodermatoses Necker Enfants Malades Hospital Paris

3. Department of Dermatology, Referral Center for Genodermatoses Saint Louis HospitalAPHP Paris France

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.19752

Reference8 articles.

1. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

2. Junctional Epidermolysis Bullosa: Allelic Heterogeneity and Mutation Stratification for Precision Medicine

3. Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa

4. Age and etiology of childhood epidermolysis bullosa mortality

5. Extracutaneous manifestations and complications of inherited epidermolysis bullosa

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