Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family-Reference-Cited by-同舟云学术

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

Published:1998-12 Issue:12 Volume:82 Page:1509-1513
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Hwang Tae-Hong,Lee Won-Ha,Kimura Akinori,Satoh Manatsu,Nakamura Takeyuki,Kim Myung-Kon,Choi Suk-Ku,Park Jeong-Euy

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference22 articles.

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2. A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11–q12;Solomon;Am J Hum Genet,1990

3. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy;Watkins;N Engl J Med,1992

4. Prognostic implications of novel β-cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy;Anan;J Clin Invest,1994

5. Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the β-myosin heavy chain gene;Epstein;Circulation,1992

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