Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.-Reference-Cited by-同舟云学术

Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

Published:1993-02-01 Issue:2 Volume:69 Page:136-141
ISSN:1355-6037
Container-title:Heart
language:en
Short-container-title:Heart

Author:

al-Mahdawi S,Chamberlain S,Cleland J,Nihoyannopoulos P,Gilligan D,French J,Choudhury L,Williamson R,Oakley C

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference34 articles.

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2. The current status of myocardial disarray in hypertrophic cardiomyopathy;Davies, M.J.;Br Heart J,1984

3. Sudden death in hypertrophic cardiomyopathy: a profile of 78 patients;Maron, B.J.; Roberts, W.E.; Epstein, S.E.;Circulation

4. Hypertrophic cardiomyopathy: an important cause of sudden death;McKenna, W.J.; Deanfield, J.E.;Arch Dis Child

5. Familial prevalence and genetic transmission of idiopathic hypertrophic cardiomyopathy;Clark, C.E.; Henry, W.L.; Epstein, S.E.;N Engl J Med

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1. Clinical utility of genetic tests for inherited hypertrophic and dilated cardiomyopathies;Cardiovascular Ultrasound;2008-12

2. Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy;Clinical Genetics;2003-09-15

3. Molecular mechanisms regulating the myofilament response to Ca2+: Implications of mutations causal for familial hypertrophic cardiomyopathy;Alterations of Excitation-Contraction Coupling in the Failing Human Heart;1998

4. Hypertrophic Cardiomyopathy: valuation and Treatment of Patients at High Risk for Sudden Death;Pacing and Clinical Electrophysiology;1997-02

5. Molecular mechanisms regulating the myofilament response to Ca2+: Implications of mutations causal for familial hypertrophic cardiomyopathy;Basic Research in Cardiology;1997