Novel and recurrent mutations in Keratin 5 and 14 in Korean patients with Epidermolysis bullosa simplex
Author:
Publisher
Elsevier BV
Subject
Dermatology,Molecular Biology,Biochemistry
Reference34 articles.
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2. The clinical spectrum of Epidermolysis bullosa simplex;Horn;Br J Dermatol,2000
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4. Keratin function in skin epithelia: a broadening palette with surprising shades;Gu;Curr Opin Cell Biol,2007
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4. Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p.Ile377Thr in keratin 14 and p.Gly138Glu in keratin 5;Experimental Dermatology;2020-09-22
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