Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6).
Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, Sticht H, Rauch A, Puleo C, Hu D, Barajas-Martinez H, Antzelevitch C, Lüscher TF, Abriel H, Duru F.
Templin C, et al. Among authors: ghadri jr.
Eur Heart J. 2011 May;32(9):1077-88. doi: 10.1093/eurheartj/ehr076. Epub 2011 Mar 7.
Eur Heart J. 2011.
PMID: 21383000
Free PMC article.