Wahidullah Mansoor

Molecular Characterization of two NR2F2 Exons identifies a Rare Intronic Variant Enriched in Indonesian Congenital Heart Disease Patients

Background: Congenital heart disease is a globally prevalent congenital disorder that has a complicated genetic etiology that includes both coding and non-coding variants. Although there is much evidence of pathogenic coding variants in key transcription factors, the role of regulatory variants in the Indonesian popula...