A Homozygous Nonsense Mutation in the Human Desmocollin-3 (DSC3) Gene Underlies Hereditary Hypotrichosis and Recurrent Skin Vesicles
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
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3. Genetic evidence for a novel human desmosomal cadherin, desmoglein 4;Whittock;J. Invest. Dermatol.,2003
4. Mutations in the plakophillin 1 gene result in ectodermal dysplasia/skin fragility syndrome;McGrath;Nat. Genet.,1997
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