A case of long QT syndrome having compound mutations of KCNH2 and SCN5A.
Ito S, Taketani T, Sugamori T, Okada T, Sato H, Adachi T, Takeda M, Kodani N, Takahashi N, Endo A, Yoshitomi H, Tanabe K, Shimizu W.
Ito S, et al.
J Cardiol Cases. 2012 Sep 19;6(6):e170-e172. doi: 10.1016/j.jccase.2012.07.004. eCollection 2012 Dec.
J Cardiol Cases. 2012.
PMID: 30533098
Free PMC article.