Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.
Wooten EC, Hebl VB, Wolf MJ et al.
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Abstract
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Incomplete penetrance and variable expression of hypertrophic cardiomyopathy (HCM) is well appreciated. Common genetic polymorphisms variants that may affect HCM penetrance and expression have been predicted but are not well established.
174 European ancestry cases, 823 European ancestry controls
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