<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)

The Role of GPD1L in the Pathogenesis of Brugada Syndrome

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