. . . . . . . "[The 828C-- > G mutation causes a substitution of a glycine for an alanine residue in the HS1-BP3 protein/was found in 2 unrelated patients with familial essential tremor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:50+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .