. . . . . . . . . . . . "[The disorder has previously been described in a family with an `autosomal dominant myopathy, with joint contractures, ophthalmoplegia, and rimmed vacuoles.` Linkage analysis and radiation hybrid mapping showed that the gene locus (Human Genome Map locus name: IBM3) is situated in a 2-Mb region of chromosome 17p13, where also a cluster of MyHC genes is located.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:38:46+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .