Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy

Published:2004-01 Issue:1 Volume:313 Page:178-184
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Hayashi Takeharu,Arimura Takuro,Ueda Kazuo,Shibata Hiroki,Hohda Shigeru,Takahashi Megumi,Hori Hisae,Koga Yoshinori,Oka Naoki,Imaizumi Tsutomu,Yasunami Michio,Kimura Akinori

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference30 articles.

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4. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy;Kamisago;New Engl. J. Med.,2000

5. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy;Gerull;Nat. Genet.,2002

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