Referenced in: none

Automatically associated channels: Kv11.1 , Kv7.1

Title: A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome.

Authors: Lia Crotti, Marzena A Lewandowska, Peter J Schwartz, Roberto Insolia, Matteo Pedrazzini, Erica Bussani, Federica Dagradi, Alfred L George, Franco Pagani

Journal, date & volume: Heart Rhythm, 2009 Feb , 6, 212-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19187913

Abstract