A systematic review and meta-analysis of genotype–phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations-Reference-Cited by-同舟云学术

A systematic review and meta-analysis of genotype–phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations

Published:2013-05-14 Issue:24 Volume:99 Page:1800-1811
ISSN:1355-6037
Container-title:Heart
language:en
Short-container-title:Heart

Author:

Lopes Luís R,Rahman M Shafiqur,Elliott Perry M

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference85 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 the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy;Watkins;Nat Genet,1995

5. Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere;Thierfelder;Cell,1994

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