Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy-Reference-Cited by-同舟云学术

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

Published:2008-07 Issue:1 Volume:156 Page:161-169
ISSN:0002-8703
Container-title:American Heart Journal
language:en
Short-container-title:American Heart Journal

Author:

Parks Sharie B.,Kushner Jessica D.,Nauman Deirdre,Burgess Donna,Ludwigsen Susan,Peterson Amanda,Li Duanxiang,Jakobs Petra,Litt Michael,Porter Charles B.,Rahko Peter S.,Hershberger Ray E.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference27 articles.

1. Clinical and genetic issues in familial dilated cardiomyopathy;Burkett;J Am Coll Cardiol,2005

2. Genetic causes of human heart failure;Morita;J Clin Invest,2005

3. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N Engl J Med,1999

4. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement;Brodsky;Circ,2000

5. High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation;Becane;Pacing Clin Electrophysiol,2000

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