The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy-Reference-Cited by-同舟云学术

The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy

Published:2008-04-14 Issue:3 Volume:79 Page:481-491
ISSN:1755-3245
Container-title:Cardiovascular Research
language:en
Short-container-title:

Author:

Jacques Adam M.,Briceno Natalia,Messer Andrew E.,Gallon Clare E.,Jalilzadeh Shapour,Garcia Edwin,Kikonda-Kanda Gaelle,Goddard Jennifer,Harding Sian E.,Watkins Hugh,Esteban M. Tomé,Tsang Victor T.,McKenna William J.,Marston Steven B.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Link

http://academic.oup.com/cardiovascres/article-pdf/79/3/481/17391583/cvn094.pdf

Reference40 articles.

1. Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy;Redwood;Cardiovasc Res,1999

2. Hypertrophic cardiomyopathy distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy;Richard;Circulation,2003

3. Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy;Van Driest;J Am Coll Cardiol,2004

4. Myosin-binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy;Van Driest;J Am Coll Cardiol,2004

5. Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy;Knollmann;Trends Cardiovasc Med,2001

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