Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain
Author:
Publisher
Elsevier BV
Subject
Dermatology,Molecular Biology,Biochemistry
Reference10 articles.
1. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism;Giebel;Proc Natl Acad Sci U S A,1991
2. Deletion of the c-kit protooncogene in the human developmental defect piebald trait;Fleischman;Proc Natl Acad Sci U S A,1991
3. Structure of a c-kit product complex reveals the basis for kinase transactivation;Mol;J Biol Chem,2003
4. New KIT mutations in patients with piebaldism;Murakami;J Dermatol Sci,2004
5. Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT;Narita;Eur J Dermatol,2011
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3. In-frame Val 216 -Ser 217 deletion of KIT in mild piebaldism causes aberrant secretion and SCF response;Journal of Dermatological Science;2018-07
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