Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders - Wikidata - wikimedia - TriplyDB

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

http://www.wikidata.org/entity/Q28069859

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Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

http://www.wikidata.org/entity/Q28069859

description

2016 nî lūn-bûn

@nan

2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@ast

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@en

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@nl

type

label

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@ast

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@en

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@nl

prefLabel

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@ast

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@en

Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@nl

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Clinical Medicine Insights. Cardiology

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Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders

@en

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Claudia Stoellberger

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

Josef Finsterer

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

P2860

TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy

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

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

Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves

Mutations with pathogenic potential in proteins located in or at the composite junctions of the intercalated disk connecting mammalian cardiomyocytes: a reference thesaurus for arrhythmogenic cardiomyopathies and for Naxos and Carvajal diseases

Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy

TMEM43 mutation p.S358L alters intercalated disc protein expression and reduces conduction velocity in arrhythmogenic right ventricular cardiomyopathy

Structure and function of desmosomal proteins and their role in development and disease

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173-180

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scholarly article

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2902843

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10.4137/CMC.S38446

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10

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2016-10-19T00:00:00Z

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27790050

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5072460

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