Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.
Amnah Y BdierSaleh Al-GhamdiPrashant K VermaKhalid DagririBandar AlshehriOmamah A JimanSherif E AhmedArthur A M WildeZahurul A BhuiyanJumana Y Al-AamaPublished in: Molecular genetics & genomic medicine (2017)
To the best of our knowledge, this is the first description of a large series of patients with familial autosomal recessive LQT, type 1. These mutations could be used for targeted screening in cardiac arrhythmia patients in Saudi Arabia and in people of Arabic ancestry.