J Shen

Spectrum of Mutations in Long-QT Syndrome Genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

A J Moss, S. Priori, A. Moss, 2000, Circulation.

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

M. Keating, I. Splawski, K. Timothy, 1998, Genomics.

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

S. Priori, P. Schwartz, G. Vincent, 1995, Human molecular genetics.

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.

M. Sanguinetti, M. Curran, M. Keating, 1996, Nature.