[N985Y mutation segregated with the phenotype from 1 Chinese family with mild and late-onset autosomal dominant retinitis pigmentosa (ADRP) a finding that has not been documented in other races.]. 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