. . . . . . . "[A novel mutation, c.2848 _ 2849delGA in OPA1, was identified in a Chinese family with (autosomal dominant optic atrophy) ADOA/mutation is associated with hearing loss, but likely not high myopia.]. 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 . "2017-10-17T13:15:07+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .