Study

Genetic Etiology of Heterotaxy

Study ID Alternative Stable ID Type
phs001691 Case Set

Study Description

To understand the genetic etiology of heterotaxy, patients with heterotaxy were consented and recruited, with blood drawn for DNA extraction and exome sequencing. Using the exome sequencing dataset obtained, rare coding sequence variants were identified.

Archive Link Archive Accession
dbGaP phs001691

Who archives the data?

There are no publications available