https://www.selleckchem.com/pr....oducts/rg2833-rgfp10
Familial dilated cardiomyopathy (DCM) is typically a monogenic disorder with dominant inheritance. Although over 40 genes have been linked to DCM, more than half of the patients undergoing comprehensive genetic testing are left without molecular diagnosis. Recently, biallelic protein-truncating variants (PTVs) in the nebulin-related anchoring protein gene (NRAP) were identified in a few patients with sporadic DCM. We determined the frequency of rare NRAP variants in a cohort of DCM patients and control patients to further evaluat
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