A systematic review and meta-analysis of genotype–phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations
Author:
Publisher
BMJ
Subject
Cardiology and Cardiovascular Medicine
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5. Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere;Thierfelder;Cell,1994
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