. . . . . . . . . . . . "[Heterozygous mutations in the gene for the Kit transmembrane receptor have been identified recently in human piebaldism and mouse 'dominant spotting.' Interestingly, all of the 14 known missense mutations that cause depigmentation in these species map to the tyrosine kinase domain of the receptor, whereas none have involved the extracellular ligand-binding domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2015-02-27"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2015-08-25T14:45:48+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .