Whole genome sequence: cardiomyopathy, 1 myotonic dystrophy patient

In this study, we analyzed the genomic information by whole genome sequencing using peripheral blood samples from patients with various cardiovascular diseases including severe heart failure to identify genetic variants related to the pathology of cardiovascular diseases. The purpose is to elucidate the underlying mechanism and develop new therapeutic interventions for cardiovascular disease.

• Type: Whole Genome Sequencing
• Archiver: Japanese Genotype-phenotype Archive (JGA)