[Two novel mutations in OA1 gene were identified in two families with ocular albinism/mutations are likely loss-of-function mutations/in OA1 gene are associated with majority of X-linked ocular albinism cases.]. 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