[a novel and rare 1 bp insertion/nonsense mutation c1378 _ 1379insG (exon 12) and the entire deletion of exon 7 in early-onset Parkinson's disease.]. 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