. . . . . . . . . . . . "[Heterozygous mutations in MYH7 encoding beta-myosin heavy chain are the most common causes of FHC, and we proposed that enhanced mutant actin-myosin function is the causative molecular abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:45:16+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .