. . . . . . . "[In the present study, the entire coding sequences and flanking regions of 12�major disease�(cardiomyopathy)-related genes [namely myosin, heavy chain�7, cardiac muscle,�?�(MYH7); myosin binding protein�C, cardiac�(MYBPC3); lamin A/C�(LMNA); troponin�I type�3�(cardiac)�(TNNI3); troponin�T type�2 (cardiac)�(TNNT2); actin,�?, cardiac muscle�1�(ACTC1); tropomyosin�1�(?)�(TPM1); sodium channel, voltage gated, type�V alpha subunit�(SCN5A); myosin, light chain�2, regulatory, cardiac, slow�(MYL2); myosin, heavy chain�6, cardiac muscle,�?�(MYH6); myosin, light chain�3, alkali, ventricular, skeletal, slow�(MYL3); and protein kinase, AMP-activated, gamma�2 non-catalytic subunit �(PRKAG2)] in 8�patients with dilated cardiomyopathy�(DCM) and in 8�patients with hypertrophic cardiomyopathy�(HCM) were amplified and then sequenced using the Ion Torrent Personal Genome Machine�(PGM) system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:14:52+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .