Peeling Skin Syndrome: Genetic Defects in Late Terminal Differentiation of the Epidermis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference21 articles.
1. Localized peeling skin syndrome: case report with ultrastructural study;Brusasco;Br J Dermatol,1998
2. A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome;Cassidy;Am J Hum Genet,2005
3. Homo-oligomerization of human corneodesmosin is mediated by its N-terminal glycine loop domain;Caubet;J Invest Dermatol,2004
4. Skin shedding (keratolysis exfoliativa congenita): report of a case;Fox;Arch Dermatol Syph,1921
5. A 4.2 upstream region of the human corneodesmosin gene directs site-specific expression in hair follicles and hyperkeratotic epidermis of transgenic mice;Gallinaro;J Invest Dermatol,2004
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