LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current. - Wikidata - wikimedia - TriplyDB

LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.

LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.

http://www.wikidata.org/entity/Q35232662

about

KCNE genetics and pharmacogenomics in cardiac arrhythmias: much ado about nothing?Modification by KCNE1 variants of the hERG potassium channel response to premature stimulation and to pharmacological inhibition.Long QT syndrome: beyond the causal mutation.Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing.

P2860

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P2860

LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.

http://www.wikidata.org/entity/Q35232662

description

2011 nî lūn-bûn

@nan

2011 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current.

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LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current.

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type

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LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current.

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LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current.

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LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current.

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LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current.

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LQT5 masquerading as LQT2: a d ...... polymorphism on KCNH2 current

@en

P2093

David Bar-Lev

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

Elena Burashnikov

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

Eyal Nof

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

Gabriel Caceres

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

Gail Rosenfeld

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

Hector Barajas-Martinez

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

Janire Urrutia

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

Micha Feinberg

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

Michael Eldar

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

Michael Glikson

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

P2860

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome

Identification of a Kir3.4 mutation in congenital long QT syndrome

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients

A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation.

Risk stratification in the long-QT syndrome.

P304

1478-1483

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scholarly article

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10.1093/EUROPACE/EUR184

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10

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13

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Charles Antzelevitch

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2011-06-28T00:00:00Z

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51451162

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21712262

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3180238

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