(Q52914429)

English

Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy.

scientific article published in December 2008

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scholarly article

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy. (English)

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

author name string

Maximilian G Posch

1

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Matthias J Posch

2

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Andreas Perrot

3

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Rainer Dietz

4

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Cemil Ozcelik

5

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

publication date

1 December 2008

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Nature Clinical Practice Cardiovascular Medicine

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

5

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

12

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

E1

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1434

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1434

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1434

7 January 2021

based on heuristic

inferred from DOI database lookup

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1434

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NCPCARDIO1434

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

1 reference

Europe PubMed Central

9 May 2018

http://europepmc.org/abstract/MED/19039334

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