Results 181 to 190 of about 6,642 (199)

Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndrome.

Europace, 2023
Takanori Aizawa, Eri T Kato, Yuko Wada
exaly  

KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort

Life, 2022
Isaac Pascual, Alicia Perez Perez, César Morís   +2 more
exaly  

Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia

Genes, 2022
Andy Schumann, Thomas W Mühleisen, Karl-Jürgen Bär   +2 more
exaly  

Gene symbol: KCNH2.

Human genetics, 2007
Crotti L, Insolia R, Pedrazzini M, Andreoli C, Gabanti E, Moncalvo C, Crimi G, De Ferrari G, Schwartz PJ.   +8 more
openaire   +3 more sources

KCNH2 gene mutation: a potential link between epilepsy and long QT-2 syndrome.

Journal of Neurogenetics, 2012
Antonio López Farré, José J Zamorano-León   +1 more
exaly  

Gene symbol: KCNH2. Disease: Long QT syndrome.

Human genetics, 2008
Crotti, L, Pedrazzini, M, Ferrandi, C, Insolia, R, Cuoretti, A, Dagradi, F, Crimi, G, Coto, E, Reguero, JR, Schwartz, PJ.   +9 more
openaire   +5 more sources

The KCNH2 gene is associated with neurocognition and the risk of schizophrenia

World Journal of Biological Psychiatry, 2013
Takashi Morihara, Masatoshi Takeda, Kazutaka Ohi   +2 more
exaly  

Role of a KCNH2 polymorphism (R1047 L) in dofetilide-induced

Journal of Molecular and Cellular Cardiology, 2004
Z SUN, P MILOS, J THOMPSON, D LLOYD, A MANKSEYMOUR, J RICHMOND, J CORDES, J ZHOU   +7 more
openaire   +1 more source

Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing

Annals of Human Genetics, 2020

exaly  

Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr-IKs α-subunit interaction

Heart Rhythm, 2009
Flavien Charpentier, Ralf P Brandes
exaly