Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation
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Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillationDPPX potassium channel antibody: frequency, clinical accompaniments, and outcomes in 20 patients.Genetics of sudden cardiac death syndromesDipeptidyl peptidase-like protein 6 is required for normal electrophysiological properties of cerebellar granule cellsA young man with near-syncopeThe role of ion channelopathies in sudden cardiac death: implications for clinical practice.Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder.The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease.A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation.The quest for the identification of genetic variants in unexplained cardiac arrest and idiopathic ventricular fibrillation.A new TASK for Dipeptidyl Peptidase-like Protein 6.Interlocus gene conversion explains at least 2.7% of single nucleotide variants in human segmental duplications.Unique cardiac Purkinje fiber transient outward current β-subunit composition: a potential molecular link to idiopathic ventricular fibrillation.Follow-up association study of linkage regions reveals multiple candidate genes for carotid plaque in Dominicans.Use of whole exome sequencing for the identification of Ito-based arrhythmia mechanism and therapy.Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained deathCellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome.Inverted low-copy repeats and genome instability--a genome-wide analysisGenetics and cardiac channelopathies.Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.Genetic Basis of Ventricular Arrhythmias.Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6Genetic etiology and evaluation of sudden cardiac death.Genetic testing for inherited cardiac disease.Misinterpretation of the mouse ECG: 'musing the waves of Mus musculus'.Transmural gradients in ion channel and auxiliary subunit expression.Genomic Study of Cardiovascular Continuum Comorbidity.Heterospecific SNP diversity in humans and rhesus macaque (Macaca mulatta).Recurrent and founder mutations in inherited cardiac diseases in the Netherlands.From whole exome sequencing to patient-specific therapy: another example of how basic research pays off in patient care.Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement.Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.DPP6 gene disruption in a family with Gilles de la Tourette syndrome.Cardiac arrhythmia and neuroexcitability gene variants in resected brain tissue from patients with sudden unexpected death in epilepsy (SUDEP).Implication of LRRC4C and DPP6 in neurodevelopmental disorders.Mapping and Ablation of Idiopathic Ventricular Fibrillation
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P2860
Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 12 March 2009
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Haplotype-sharing analysis imp ...... athic ventricular fibrillation
@en
Haplotype-sharing analysis imp ...... thic ventricular fibrillation.
@nl
type
label
Haplotype-sharing analysis imp ...... athic ventricular fibrillation
@en
Haplotype-sharing analysis imp ...... thic ventricular fibrillation.
@nl
prefLabel
Haplotype-sharing analysis imp ...... athic ventricular fibrillation
@en
Haplotype-sharing analysis imp ...... thic ventricular fibrillation.
@nl
P2093
P2860
P50
P1476
Haplotype-sharing analysis imp ...... athic ventricular fibrillation
@en
P2093
Connie R Bezzina
Imke Christiaans
Karel T Koch
Leander Beekman
Marcel M A M Mannens
Marielle Alders
Pieter G Postema
Sophie Demolombe
Tamara T Koopmann
P2860
P304
P356
10.1016/J.AJHG.2009.02.009
P407
P577
2009-03-12T00:00:00Z