[A missense mutation of Tyr486Asp in the UGT1A1 gene is considered to be the cause of the Crigler-Najjar syndrome type II in this patient/is a recessive trait that is autosomally inherited in this family.]. 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