Results 191 to 199 of about 6,642 (199)

Most LQT-linked KCNH2 mutations are trafficking-defective

Heart Rhythm, 2005
Brian P. Delisle, Corey L. Anderson, Blake D. Anson, Jennifer A. Kilby, Melissa L. Will, David J. Tester, Michael J. Ackerman, Qiuming Gong, Zhengfeng Zhou, Craig T. January   +9 more
openaire   +1 more source

KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population†‡

Human Mutation, 2002
Kang Ying, Cuilan Li, Wenling Liu
exaly  

Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death

Epilepsia, 2013
Oscar Campuzano, Federico Zara
exaly  

Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano–Ward syndrome under double mutations and acquired long QT syndrome under heterozygote

Journal of Cardiology, 2017
Yuko Wada, Daisuke Fukumoto, Keiko Sonoda   +2 more
exaly  

AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndrome Open Access

European Heart Journal
Fabien Praz
exaly  

Gain-of-Function KCNH2 Mutations in Patients with Brugada Syndrome

Journal of Cardiovascular Electrophysiology, 2014
Hideki Itoh
exaly  

KCNH2: Role in Cardiac Physiology and Pathophysiology

openaire   +1 more source

SCHIZOPHRENIA-RELATED ISOFORM OF KCNH2 AND DEVELOPMENT OF ANTIPSYCHOTIC DRUGS

2009
WEINBERGER DANIEL R, HUFFAKER STEPHEN J, KLEINMAN JOEL E, LU BAI   +3 more
openaire   +2 more sources

Gene Symbol: KCNH2 Disease: Long QT syndrome

2007
Crotti, L, Pedrazzini, M, Ferrandi, C, Insolia, R, Tosin, L, Vicentini, A, Turco, A, De Ferrari, GM, Schwartz, PJ   +8 more
openaire   +1 more source