Molecular mechanisms of inherited arrhythmias. - Wikidata - awgldk - TriplyDB

Molecular mechanisms of inherited arrhythmias.

Molecular mechanisms of inherited arrhythmias.

http://www.wikidata.org/entity/Q37480777

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Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias.Animal models of arrhythmogenic cardiomyopathy.Evaluation and management of bradycardia in neonates and children.

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P2860

Molecular mechanisms of inherited arrhythmias.

http://www.wikidata.org/entity/Q37480777

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on May 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Molecular mechanisms of inherited arrhythmias.

@en

Molecular mechanisms of inherited arrhythmias.

@nl

type

label

Molecular mechanisms of inherited arrhythmias.

@en

Molecular mechanisms of inherited arrhythmias.

@nl

prefLabel

Molecular mechanisms of inherited arrhythmias.

@en

Molecular mechanisms of inherited arrhythmias.

@nl

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138920208784340768

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Current Genomics

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Molecular mechanisms of inherited arrhythmias.

@en

P2093

Charles I Berul

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Cordula M Wolf

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P2860

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

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

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

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

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

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

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

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160-168

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scholarly article

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10.2174/138920208784340768

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3

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9

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2008-05-01T00:00:00Z

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24425656

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2679644

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