A c-kit Mutation in Exon 18 in Familial Mastocytosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference11 articles.
1. Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations;Bodemer;J Invest Dermatol,2010
2. Somatic and germline genetics at the JAK2 locus;Campbell;Nat Genet,2009
3. Mast cell activation syndrome: a newly recognized disorder with systemic clinical manifestations;Hamilton;J Allergy Clin Immunol,2011
4. Mutation D816V alters the internal structure and dynamics of c-KIT receptor cytoplasmic region: implications for dimerization and activation mechanisms;Laine;PLoS Comput Biol,2011
5. Phenotypic and genotypic characteristics of mastocytosis according to the age of onset;Lanternier;PLoS One,2008
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