Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform.

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Sodium channel biophysics, late sodium current and genetic arrhythmic syndromes

P2860

Q33708707-63E1CF24-66DC-4C0F-AD49-37497332A7B1

P2860

Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform.

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http://www.wikidata.org/entity/Q43142639

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2011 nî lūn-bûn

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2011年の論文

@ja

2011年学术文章

@wuu

2011年学术文章

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2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

2011年學術文章

@zh-hant

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Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@en

Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@nl

type

Item

label

Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@en

Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@nl

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Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@en

Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@nl

P1476

Enhanced impact of SCN5A mutat ...... drome in fetal splice isoform.

@en

P2093

Tiannan Wang

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P2860

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.

A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations

Molecular mechanism for an inherited cardiac arrhythmia.

Cardiac sodium channelopathies.

Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome.

Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia

Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.

The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel.

Alternative splicing of Nav1.5: an electrophysiological comparison of 'neonatal' and 'adult' isoforms and critical involvement of a lysine residue.

P304

598-599

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P31

scholarly article

editorial

P356

10.1016/J.HRTHM.2011.11.049

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P433

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

P478

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

P50

Xander H T Wehrens

P577

2011-11-30T00:00:00Z

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P5875

51850325

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P698

22138134

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P932

4324321

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Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform.

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P2860

P2860

Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932