Genome Sequencing and Variant Calling of HCM Patients with MYH7 Variants

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Platforms

dbGaP

View in dbGaP

phs004024.v1.p1

APIs

Consent Codes

DS-CMP-IRB

Focus / Diseases

Cardiomyopathy, Hypertrophic

Study Design

Case Set

Data Types

SNP/CNV Genotypes (NGS)

Subjects

48