<p>To investigate potential genetic causes of cardiomyopathy we recruited 48 patients harboring rare <a href="https://www.ncbi.nlm.nih.gov/gene/4625">MYH7</a> variants identified from panel-based testing and with a clinical manifestation of cardiomyopathy. Genome sequencing was performed to identify other potential causative variants and genetic modifiers of the cardiomyopathy phenotype, which varied among patients.</p>

Genome Sequencing and Variant Calling of HCM Patients with MYH7 Variants

Cardiomyopathy, Hypertrophic study with SNP/CNV Genotypes (NGS) data on dbGaP (48 participants)