Vinculin variant M94I identified in sudden unexplained nocturnal death syndrome decreases cardiac sodium current. - Wikidata - awgldk - TriplyDB

Vinculin variant M94I identified in sudden unexplained nocturnal death syndrome decreases cardiac sodium current.

Vinculin variant M94I identified in sudden unexplained nocturnal death syndrome decreases cardiac sodium current.

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An East Asian Common Variant Vinculin P.Asp841His Was Associated With Sudden Unexplained Nocturnal Death Syndrome in the Chinese Han Population.Sudden Unexplained Nocturnal Death Syndrome: The Hundred Years' Enigma.

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Vinculin variant M94I identified in sudden unexplained nocturnal death syndrome decreases cardiac sodium current.

http://www.wikidata.org/entity/Q37652669

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 20 February 2017

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Vinculin variant M94I identifi ...... reases cardiac sodium current.

@en

Vinculin variant M94I identifi ...... reases cardiac sodium current.

@nl

type

label

Vinculin variant M94I identifi ...... reases cardiac sodium current.

@en

Vinculin variant M94I identifi ...... reases cardiac sodium current.

@nl

prefLabel

Vinculin variant M94I identifi ...... reases cardiac sodium current.

@en

Vinculin variant M94I identifi ...... reases cardiac sodium current.

@nl

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Scientific Reports

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Vinculin variant M94I identifi ...... creases cardiac sodium current

@en

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Brandi Wiedmeyer

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

Jianding Cheng

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

John W Kyle

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

Jonathan C Makielski

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

Ravi Vaidyanathan

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

P2860

Cardiac-myocyte-specific excision of the vinculin gene disrupts cellular junctions, causing sudden death or dilated cardiomyopathy

Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and F

Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype

Vinculin directly binds zonula occludens-1 and is essential for stabilizing connexin-43-containing gap junctions in cardiac myocytes

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

High purity human-induced pluripotent stem cell-derived cardiomyocytes: electrophysiological properties of action potentials and ionic currents.

Sudden unexplained death syndrome in north-east Thailand.

Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin.

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

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scholarly article

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10.1038/SREP42953

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28218286

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5317164

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