. . . . . . . "[Myotilin S55F mutations may cause a clinically distinct autosomal-dominant late-onset and lower-limb distal myopathic syndrome/helps to depict the topography of fatty muscle atrophy and to detect gene mutation carriers.]. 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 . "2017-10-17T13:17:45+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .