[this study reports the presence of a G691R mutation in exon 7 of the ATP7B gene of a Lebanese family with WD patients/affected members were homozygous for this mutation and had liver disease ranging from subclinical hepatitis to advanced cirrhosis.]. 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