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Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2

Crossref DOI link: https://doi.org/10.1016/j.jacbts.2018.12.001

Published Print: 2019-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Abdelfatah, Nelly

Chen, Ruping

Duff, Henry J.

Seifer, Colette M.

Buffo, Ilan

Huculak, Cathleen

Clarke, Stephanie

Clegg, Robin

Jassal, Davinder S.

Gordon, Paul M.K.

Ober, Carole

Frosk, Patrick

Gerull, Brenda
Funding

Funding for this research was provided by:

Cumming School of Medicine, University of Calgary

Ministry of Economic Development and Trade, Government of Alberta
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Text and Data Mining valid from 2019-04-01

Text and Data Mining valid from 2019-04-01

Version of Record valid from 2018-12-11
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This article is maintained by: Elsevier

Article Title: Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2

Journal Title: JACC: Basic to Translational Science

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.jacbts.2018.12.001

Content Type: article

Copyright: © 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.