. . . . . . . "[In a 3-generation ataxic family with the m.8993T-- > C mutation of mtDNA, 1 had episodic ataxia & transient hemipareses, broadening the phenotype/further cases were identified in an additional cohort of 191 patients with suspected EA.]. 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 . "2017-10-17T13:14:44+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .