Intraepidermal collagen type VII in dystrophic epidermolysis bullosa: report of five new cases
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.1992.tb00649.x/fullpdf
Reference10 articles.
1. Type VII collagen is a major structural component of anchoring fibrils.
2. Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosis
3. Type VII Collagen is a Normal Component of Epidermal Basement Membrane, Which Shows Altered Expression in Recessive Dystrophic Epidermolysis Bullosa
4. Intraepidermal type VII collagen
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1. Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub‐classification of inherited epidermolysis bullosa: a single‐centre retrospective comparative study of 87 cases with long‐term follow‐up;Journal of the European Academy of Dermatology and Venereology;2021-02-05
2. Self‐improving dystrophic epidermolysis bullosa: First report of clinical, molecular, and genetic characterization of five patients from Southeast Asia;American Journal of Medical Genetics Part A;2020-11-30
3. Intraepidermal Type VII Collagen by Immunofluorescence Mapping: A Specific Finding for Bullous Dermolysis of the Newborn;Pediatric Dermatology;2017-05
4. Recessive Bullous Dermolysis of the Newborn in Preterm Siblings with a Missense Mutation in Type VII Collagen;Pediatric Dermatology;2015-01-30
5. Frequent Occurrence of Aplasia Cutis Congenita in Bullous Dermolysis of the Newborn;Acta Dermato Venereologica;2014
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