Deletion of theKIT andPDGFRA genes in a patient with piebaldism
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference38 articles.
1. A patient with an interstitial deletion of the proximal portion of the long arm of chromosome 4
2. Electron Microscopy of Melanocytes in Human Piebaldism*
3. The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus
4. cDNA cloning and expression of the human A-type platelet-derived growth factor (PDGF) receptor establishes structural similarity to the B-type PDGF receptor.
5. Familial white skin spotting (piebaldness) (“partial albinism”) with white forelock
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1. Genetic Etiology of Renal Agenesis: Fine Mapping of Renag1 and Identification of Kit as the Candidate Functional Gene;PLOS ONE;2015-02-18
2. A novel mutation of KIT gene results in piebaldism in a Chinese family;Journal of the European Academy of Dermatology and Venereology;2014-09-08
3. Piebaldism;The Journal of Dermatology;2012-06-01
4. A Novel Kit Gene Mutation in CF1 Mice Involved in the Extracellular Domain of the KIT Protein;Experimental Animals;2012
5. Transplante de melanócitos no piebaldismo: relato de caso;Anais Brasileiros de Dermatologia;2010-06
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