Genotype–phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin-Reference-Cited by-同舟云学术

Genotype–phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin

Published:2006-05 Issue:1 Volume:88 Page:78-85
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Bos J. Martijn,Poley Rainer N.,Ny Melissa,Tester David J.,Xu Xiaolei,Vatta Matteo,Towbin Jeffrey A.,Gersh Bernard J.,Ommen Steve R.,Ackerman Michael J.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference36 articles.

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3. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation;Geisterfer-Lowrance;Cell,1990

4. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle;Poetter;Nat. Genet.,1996

5. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy;Watkins;Nat. Genet.,1995

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