[3 putative A1A2 mutations (D718N, R763H, P979L) & 3 that await validation (P796R, E902K, X1021R) were found in familial hemiplegic migraine/and P979L may predispose to seizures and mental retardation/does not play a major role in sporadic HM.]. 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