Results 141 to 150 of about 2,693,618 (154)

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

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  

Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies

Heart Rhythm, 2006
Marcel M A M Mannens, Connie R Bezzina
exaly  

A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome

Heart Rhythm, 2013
Masa-Aki Kawashiri, Kenshi Hayashi
exaly  

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  

Functional analysis of KCNH2 gene mutations of type 2 long QT syndrome in larval zebrafish using microscopy and electrocardiography

Heart and Vessels, 2018
Hayato Tada, Masa-Aki Kawashiri
exaly  

Analysis of KCNH2 and CACNA1C schizophrenia risk genes on EEG functional network modulation during an auditory odd-ball task

European Archives of Psychiatry and Clinical Neuroscience, 2019
Javier Gomez-Pilar, Béquer Benjamín Cea Cañas, Jesus Poza   +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  

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

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