The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene.

Author:

al-Mahdawi S,Chamberlain S,Chojnowska L,Michalak E,Nihoyannopoulos P,Ryan M,Kusnierczyk B,French J A,Gilligan D M,Cleland J

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference22 articles.

1. Hypertrophic cardiomyopathy: Interrelations of clinical manifestations, pathophysiology and therapy;Maron, B.J.; Bonow, R.O.; RO, Cannon; HI, Leon; MB, Epstein; S.E.;N EnglJ Med,1987

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

3. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14ql;Jarcho, J.A.; McKenna, W.; Pare, J.A.P.,1989

4. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy;Watkins, H.; Rosenzweig, A.; Hwang, D.-S.; Levi, T.; McKenna, W.; Seidman, C.E.; Seidman, J.G.;N Engl J Med,1992

5. A disease locus for hypertrophic cardiomyopathy maps to chromosome lq3;Watkins, H.; McRae, C.; Thierfelder, L.;Nature Genet,1993

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