Late-onset hypertrophie cardiomyopathy caused by a mutation in the cardiac troponin t gene

New England Journal of Medicine

Volumn 341, Issue 24, 1999, Pages 1855-1856

  Elliott, Perry M ^a   Leon D'Cruz, B S ^a   Mckenna, William J ^a  

^a ST GEORGE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

TROPONIN T;

ADULT; CASE REPORT; CLINICAL FEATURE; DISEASE ACTIVITY; ECHOCARDIOGRAPHY; GENE MUTATION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LETTER; MALE; ONSET AGE; PATHOGENESIS; PHYSICAL EXAMINATION; PRIORITY JOURNAL;

AGE OF ONSET; CARDIOMYOPATHY, HYPERTROPHIC; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; TROPONIN T;

EID: 0033540007     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199912093412416     Document Type: Article

References (3)

1. Charron P, Dubourg O, Desnos M, et al. Clinical features and prognostic implications of familial hypertrophie cardiomyopathy related to the cardiac myosin-binding protein C gene. Circulation 1998;97:2230-6.
2. Niimura H, Bachinski LL, Sangwatanaroj S, et al. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophie cardiomyopathy. N Engl J Med 1998;338:1248-57.
3. Watkins H, McKenna WJ, Thierfelder L, et al. Mutations in the genes for cardiac troponin T and a-tropomyosin in hypertrophie cardiomyopathy. N Engl J Med 1995;332:1058-64.