A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.
Priori SG, Pandit SV, Rivolta I, Berenfeld O, Ronchetti E, Dhamoon A, Napolitano C, Anumonwo J, di Barletta MR, Gudapakkam S, Bosi G, Stramba-Badiale M, Jalife J.
Priori SG, et al. Among authors: jalife j.
Circ Res. 2005 Apr 15;96(7):800-7. doi: 10.1161/01.RES.0000162101.76263.8c. Epub 2005 Mar 10.
Circ Res. 2005.
PMID: 15761194