Functional consequences of anLMNAmutation associated with a new cardiac and non-cardiac phenotype-Reference-Cited by-同舟云学术

Functional consequences of anLMNAmutation associated with a new cardiac and non-cardiac phenotype

Published:2003-05 Issue:5 Volume:21 Page:473-481
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Charniot Jean-Christophe,Pascal Cécile,Bouchier Christiane,Sébillon Pascale,Salama Jeffrey,Duboscq-Bidot Laëtitia,Peuchmaurd Mireille,Desnos Michel,Artigou Jean-Yves,Komajda Michel

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease;Arbustini;J Am Coll Cardiol,2002

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

3. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy;Bonne;Nat Genet,1999

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

5. The nuclear envelope in muscular dystrophy and cardiovascular diseases;Burke;Traffic,2001

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