Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.
about
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis.Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.Long QT syndrome in South Africa: the results of comprehensive genetic screening.Inherited arrhythmic disorders in Japan.Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of SingaporePathophysiological role of omega pore current in channelopathiesRecurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.Molecular analysis of potassium ion channel genes in sudden death cases among patients administered psychotropic drug therapy: are polymorphisms in LQT genes a potential risk factor?Cloning and functional characterization of the smooth muscle ether-a-go-go-related gene K+ channel. Potential role of a conserved amino acid substitution in the S4 region.Cardiac ion channel gene mutations in Greek long QT syndrome patients.DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.Functional characterization of the C-terminus of the human ether-à-go-go-related gene K(+) channel (HERG).Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties.Long QT syndrome mutation detection by SNaPshot technique.Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2
P2860
Q24534117-2F2E2C00-9D26-450F-91C2-C7AF4BF3EC99Q33145216-52798797-29B0-474D-908F-8B0DE5A79B1BQ33157691-B86890B3-7854-4B01-B710-E61FC8F8E167Q33163516-DEBA309A-2DF1-42F1-9995-A36012117578Q35125502-78E72A41-CE85-4675-B076-91D6B637C4DEQ35827452-8ED969A7-5A39-4F9A-AD49-D2BA3E92082BQ36022793-E766E29F-F861-4CE3-B8DE-40081D4EE902Q37193903-3EDA127F-2FF9-4BD7-AFF8-2D1FD92E5732Q44028648-87ED0A0B-4A8A-40F9-9933-7D78EF2AC2FBQ44213450-C13EC17E-70D4-4512-814F-27F6A6B20EB4Q44757963-F95C6F86-51AD-4DAA-A880-24B5DD721019Q48276367-E54CA220-7089-431E-90E1-5C918E2112B4Q48883198-DF544C3A-67B8-48C0-8C60-C3B64D31FB02Q50723364-09E15E36-AB5C-4FBF-B113-C8A696CCB395Q54358787-8957C8BB-610D-485D-95A8-3A3CDF784F9EQ57807332-559DF032-5339-4F4A-99DB-03943FD157F0
P2860
Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Genomic organization and mutat ...... for familial long QT syndrome.
@ast
Genomic organization and mutat ...... for familial long QT syndrome.
@en
type
label
Genomic organization and mutat ...... for familial long QT syndrome.
@ast
Genomic organization and mutat ...... for familial long QT syndrome.
@en
prefLabel
Genomic organization and mutat ...... for familial long QT syndrome.
@ast
Genomic organization and mutat ...... for familial long QT syndrome.
@en
P2093
P356
P1433
P1476
Genomic organization and mutat ...... for familial long QT syndrome.
@en
P2093
H Sakurada
T Nakayama
T Sawayama
Y Nakamura
P2888
P304
P356
10.1007/S004390050717
P577
1998-04-01T00:00:00Z
P6179
1031676600