Keratins and skin disorders
Author:
Publisher
Wiley
Subject
Pathology and Forensic Medicine
Reference93 articles.
1. Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities;Bonifas;Science,1991
2. Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses;Coulombe;Cell,1991
3. A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering;Lane;Nature,1992
4. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation;Irvine;Br J Dermatol,1999
5. The clinical spectrum of epidermolysis bullosa simplex;Horn;Br J Dermatol,2000
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