Loss‐of‐function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype-Reference-Cited by-同舟云学术

Loss‐of‐function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

Published:2019-01-02 Issue:5 Volume:180 Page:1114-1122
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Maruthappu T.¹,Posafalvi A.¹,Castelletti S.²,Delaney P.J.¹,Syrris P.³,O'Toole E.A.¹,Green K.J.⁴,Elliott P.M.⁵,Lambiase P.D.³⁵,Tinker A.⁶,McKenna W.J.⁵,Kelsell D.P.¹^ORCID

Affiliation:

1. Blizard Institute Queen Mary University of London LondonU.K.

2. Istituto Auxologico Italiano IRCCS Center for Cardiac Arrhythmias of Genetic Origin Milan Italy

3. Institute of Cardiovascular Science University College London London U.K.

4. Department of Pathology and Dermatology Northwestern University Feinberg School of Medicine Chicago IL U.S.A.

5. Department of Cardiac Electrophysiology The Barts Heart Centre St Bartholomew's Hospital London U.K.

6. The Heart Centre Queen Mary University of London London U.K.

Funder

Medical Research Council

British Heart Foundation

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.17388

Reference25 articles.

1. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed Modification of the Task Force Criteria

2. Arrhythmogenic Cardiomyopathy

3. Role of Genetic Analysis in the Management of Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

4. Cell-cell connectivity: desmosomes and disease

5. Desmosome regulation and signaling in disease

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