Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

about

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

Item

http://www.wikidata.org/entity/Q36410506

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh

2012年學術文章

@zh-hant

name

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@ast

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@en

type

Item

label

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@ast

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@en

prefLabel

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@ast

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@en

P1476

Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.

@en

P2093

Craig T January

http://www.w3.org/2001/XMLSchema#string

Jonathan W Knoche

http://www.w3.org/2001/XMLSchema#string

Kate M Orland

http://www.w3.org/2001/XMLSchema#string

Kathleen R Maginot

http://www.w3.org/2001/XMLSchema#string

P2860

KCNQ1 gain-of-function mutation in familial atrial fibrillation

Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Risk stratification in the long-QT syndrome.

Task Force 7: arrhythmias.

Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.

Congenital long-QT syndromes: a clinical and genetic update from infancy through adulthood.

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome.

P304

124838

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1155/2012/124838

http://www.w3.org/2001/XMLSchema#string

P478

2012

http://www.w3.org/2001/XMLSchema#string

P577

2012-11-05T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

233799270

http://www.w3.org/2001/XMLSchema#string

P698

23193492

http://www.w3.org/2001/XMLSchema#string

P932

3501806

http://www.w3.org/2001/XMLSchema#string