The Genetic Basis for Cardiomyopathy

Author:

Seidman J.G.,Seidman Christine

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference65 articles.

1. MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy and heart failure;Arber;Cell,1997

2. Enteroviral protease 2A cleaves dystrophin;Badorff;Nat. Med.,1999

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

4. Bozkurt, B., and Mann, D.L. (2000). Dilated cardiomyopathy. In Cardiovascular Medicine, J.T. Willerson and J.N. Cohn, eds. (Churchill Livingstone), pp. 1034–1053.

5. Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11;Carrier;Nat. Genet.,1993

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