Abstract
Background: Myopalladin (MYPN) is a 145 kDa striated muscle-specific sarcomeric protein belonging to the palladin (PALLD)/MYPN/myotilin family of actin-associated immunoglobulin-containing proteins in the Z-line. MYPN gene mutations are causative for dilated (DCM), hypertrophic and restrictive cardiomyopathy.
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