Septal wall thinning and systolic dysfunction in patients with hypertrophic cardiomyopathy caused by a cardiac troponin I gene mutation

American Heart Journal

Volumn 143, Issue 4, 2002, Pages 690-695

  Shimizu, Masami ^a   Ino, Hidekazu ^a   Okeie, Kazuyasu ^a   Yamaguchi, Masato ^a   Hayashi, Kenshi ^a   Nagata, Mitsuru ^a   Itoh, Hideki ^a   Iwaki, Taku ^a   Oe, Kotaro ^a   Konno, Tetsuo ^a   Mabuchi, Hiroshi ^a  

^a KANAZAWA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; LYSINE; TROPONIN I;

ADULT; AGED; ARTICLE; CORRELATION ANALYSIS; DISEASE COURSE; ECHOCARDIOGRAPHY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEART DISEASE; HEART FUNCTION; HEART VENTRICLE SEPTUM; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRIORITY JOURNAL; PROGNOSIS;

EID: 0036238249     PISSN: 00028703     EISSN: None     Source Type: Journal    
DOI: 10.1067/mhj.2002.120291     Document Type: Article

References (17)

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8. Altered interactions among thin filament proteins modulate cardiac function
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