Population
Individuals with Restrictive cardiomyopathy (RCM)
Design
Review
Authors
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May support genetic screening of RCM relatives; leaves open therapeutic implications of sarcomeric mutations.
Restrictive cardiomyopathy can be caused by mutations in sarcomeric contractile protein genes, highlighting the importance of clinical and genetic screening for relatives of affected patients.
Mogensen et al. (2009) studied this question.
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