<p>This study performed exome sequencing on a proband with Brugada Syndrome, as well as high-density SNP array data from the proband, affected family members, and unaffected family members. The principal findings of this study were the identification of GPD1L-A280V as the only plausible variant present in a linkage region on chromosome 3, which co-segregated with the Brugada Syndrome phenotype in this family. Exome sequencing data of the proband, as well as SNP array data from the family, are available.<br></p>

The Role of GPD1L in the Pathogenesis of Brugada Syndrome

Brugada Syndrome study with SNP Genotypes (Array), WXS data on dbGaP (15 participants)