Mutations in the Ligand-Binding Domain of the Kit Receptor: An Uncommon Site in Human Piebaldism
- 1 November 1996
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 107 (5) , 703-706
- https://doi.org/10.1111/1523-1747.ep12365596
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Structure-function analyses of the kit receptor for the steel factorThe International Journal of Cell Cloning, 1996
- c-kit point mutation of extracellular domain in patients with myeloproliferative disordersBritish Journal of Haematology, 1995
- Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndromeHuman Molecular Genetics, 1995
- Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypesNature Genetics, 1995
- Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2Nature Genetics, 1994
- Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeNature Genetics, 1994
- Human piebald trait resulting from a dominant negative mutant allele of the c-kit membrane receptor gene.Journal of Clinical Investigation, 1992
- The Dominant W 42 Spotting Phenotype Results from a Missense Mutation in the c- kit Receptor KinaseScience, 1990
- The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locusNature, 1988
- The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic DomainsScience, 1988