A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.

A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.

Item
http://www.wikidata.org/entity/Q33155692
The KCNE2 K+ channel regulatory subunit: Ubiquitous influence, complex pathobiologyKCNE2 and the K (+) channel: the tail wagging the dogKcne2 deletion creates a multisystem syndrome predisposing to sudden cardiac deathCongenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.HERG1 channelopathiesEmerging concepts in the pharmacogenomics of arrhythmias: ion channel trafficking.Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.Novel exon 1 protein-coding regions N-terminally extend human KCNE3 and KCNE4.Augmented rififylin is a risk factor linked to aberrant cardiomyocyte function, short-QT interval and hypertension.Regulation of human cardiac potassium channels by full-length KCNE3 and KCNE4.The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome.Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.Molecular Pathophysiology of Congenital Long QT Syndrome.The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.Kcne4 deletion sex-specifically predisposes to cardiac arrhythmia via testosterone-dependent impairment of RISK/SAFE pathway induction in aged mice.
P2860

A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance.

Item
http://www.wikidata.org/entity/Q33155692
description
2007 nî lūn-bûn
@nan
2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@ast
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@en
type
label
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@ast
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@en
prefLabel
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@ast
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P5875
P698
P921
P356
P1433
P1476
A KCNE2 mutation in a patient ...... d serum electrolyte imbalance.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P5875
P698
P921