Genetic characterization of familial CPVT after 30 years.
about
A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia.Array comparative genomic hybridization identifies a heterozygous deletion of exon 3 of the RYR2 geneAbnormal Ca(2+) homeostasis, atrial arrhythmogenesis, and sinus node dysfunction in murine hearts modeling RyR2 modificationCalcium leak through ryanodine receptors leads to atrial fibrillation in 3 mouse models of catecholaminergic polymorphic ventricular tachycardia.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.A tryptophan residue in the caffeine-binding site of the ryanodine receptor regulates Ca sensitivity
P2860
Genetic characterization of familial CPVT after 30 years.
description
2009 nî lūn-bûn
@nan
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genetic characterization of familial CPVT after 30 years.
@ast
Genetic characterization of familial CPVT after 30 years.
@en
type
label
Genetic characterization of familial CPVT after 30 years.
@ast
Genetic characterization of familial CPVT after 30 years.
@en
prefLabel
Genetic characterization of familial CPVT after 30 years.
@ast
Genetic characterization of familial CPVT after 30 years.
@en
P2093
P356
P1476
Genetic characterization of familial CPVT after 30 years.
@en
P2093
D Woodrow Benson
Maully J Shah
Theresa A Beery
P356
10.1177/1099800409333369
P407
P577
2009-04-26T00:00:00Z