Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

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A novel desmin mutation causing severe left ventricular arrhythmogenic cardiomyopathy/dysplasia

P2860

Q58128759-ABE82C38-2C26-4E37-8F6C-94989C8BEEA0

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Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

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http://www.wikidata.org/entity/Q55037788

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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2017年學術文章

@zh-hant

name

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

@en

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

@nl

type

Item

label

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

@en

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

@nl

prefLabel

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

@en

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

@nl

P1476

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice

@en

P2093

Guangping Li

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

Ka Hou Christien Li

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Martin C S Wong

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

Sunny Hei Wong

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

Tong Liu

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Wing Tak Wong

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Yat Sun Chan

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P2860

Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts

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

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

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

The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14.

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

Electrophysiological Mechanisms of Gastrointestinal Arrhythmogenesis: Lessons from the Heart

Mechanisms of Electrical Activation and Conduction in the Gastrointestinal System: Lessons from Cardiac Electrophysiology

Conduction abnormalities and ventricular arrhythmogenesis: The roles of sodium channels and gap junctions

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11-22

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scholarly article

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10.1002/JOA3.12021

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

P478

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

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2017-12-21T00:00:00Z

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29721109

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P921

arrhythmogenic right ventricular cardiomyopathy

P932

5828272

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Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

about

P2860

P2860

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932