[In a mixed uveal and cutaneous melanoma family, CDKN2A is demonstrated for the first time to be a uveal melanoma (UM) susceptibility gene, loss of function of which is involved in the pathogenesis of UM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE