A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy-Reference-Cited by-同舟云学术

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A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy

Published:2002-01 Issue:1 Volume:89 Page:29-33
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Fujino Noboru,Shimizu Masami,Ino Hidekazu,Yamaguchi Masato,Yasuda Toshihiko,Nagata Mitsuru,Konno Tetsuo,Mabuchi Hiroshi

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference24 articles.

1. Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease;Solomon;J Clin Invest,1990

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

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

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

5. Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy;Watkins;N Engl J Med,1995

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