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Peripartum (PP) cardiomyopathy (CM) is a rare condition of unknown etiology that occurs in late pregnancy or early postpartum. Initial evidence suggests that genetic factors may influence PPCM. This study evaluated and replicated genome-wide association of single nucleotide polymorphisms with PPCM.

Genome-Wide Significance and Replication of the Chromosome 12p11.22 Locus Near thePTHLHGene for Peripartum Cardiomyopathy