A Common Keratin 5 Gene Mutation in Epidermolysis Bullosa Simplex–Weber-Cockayne
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference17 articles.
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3. A human keratin 14 “knockout”: the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein;Chan;Genes Dev,1994
4. Structure, function, and dynamics of keratin intermediate filaments;Steinert;J Invest Dermatol,1993
5. Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses;Coulombe;Cell,1991
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1. The Skin;Keeling’s Fetal and Neonatal Pathology;2015
2. Efficient KRT14 Targeting and Functional Characterization of Transplanted Human Keratinocytes for the Treatment of Epidermolysis Bullosa Simplex;Molecular Therapy;2010-09
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4. The vesiculobullous reaction pattern;Weedon's Skin Pathology;2010
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