KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
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Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndromeSudden cardiac death in China: current status and future perspectivesMolecular Cloning and Functional Expression of the Equine K+ Channel KV11.1 (Ether à Go-Go-Related/KCNH2 Gene) and the Regulatory Subunit KCNE2 from Equine MyocardiumMutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.Genotype-based clinical manifestation and treatment of Chinese long QT syndrome patients with KCNQ1 mutations - R380S and W305L.Phenotype guided characterization and molecular analysis of Indian patients with long QT syndromes.A dual mechanism for I(Ks) current reduction by the pathogenic mutation KCNQ1-S277L.Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm.The residue I257 at S4-S5 linker in KCNQ1 determines KCNQ1/KCNE1 channel sensitivity to 1-alkanolsAnalysis of genetic and non-genetic factors that affect the QTc interval in a Mongolian population: the GENDISCAN studyNovel mutations of KCNQ1 in Long QT syndrome.Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland.
P2860
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P2860
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
description
2002 nî lūn-bûn
@nan
2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@ast
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@en
type
label
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@ast
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@en
prefLabel
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@ast
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@en
P2093
P2860
P356
P1433
P1476
KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
@en
P2093
Cailian Kang
Junguo Yang
Shenghan Chen
Shuoyan Zhang
P2860
P304
P356
10.1002/HUMU.9085
P577
2002-12-01T00:00:00Z