A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation

Here, Michael Gollob and colleagues perform a whole exome sequencing study to identify a mutation in the atrial-specific myosin light chain gene MYL4 in a small family with autosomal dominant familial atrial fibrillation. They also test the functionality of this MYL4mutation in zebrafish cardiac fun...

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Autores principales: Nathan Orr, Rima Arnaout, Lorne J. Gula, Danna A. Spears, Peter Leong-Sit, Qiuju Li, Wadea Tarhuni, Sven Reischauer, Vijay S. Chauhan, Matthew Borkovich, Shaheen Uppal, Arnon Adler, Shaun R. Coughlin, Didier Y. R. Stainier, Michael H. Gollob
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Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/3cbe2796738e4c49b3e6beec3f1f88fe
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spelling oai:doaj.org-article:3cbe2796738e4c49b3e6beec3f1f88fe2021-12-02T15:34:56ZA mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation10.1038/ncomms113032041-1723https://doaj.org/article/3cbe2796738e4c49b3e6beec3f1f88fe2016-04-01T00:00:00Zhttps://doi.org/10.1038/ncomms11303https://doaj.org/toc/2041-1723Here, Michael Gollob and colleagues perform a whole exome sequencing study to identify a mutation in the atrial-specific myosin light chain gene MYL4 in a small family with autosomal dominant familial atrial fibrillation. They also test the functionality of this MYL4mutation in zebrafish cardiac function and recapitulate disease-related phenotypes.Nathan OrrRima ArnaoutLorne J. GulaDanna A. SpearsPeter Leong-SitQiuju LiWadea TarhuniSven ReischauerVijay S. ChauhanMatthew BorkovichShaheen UppalArnon AdlerShaun R. CoughlinDidier Y. R. StainierMichael H. GollobNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-8 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Nathan Orr
Rima Arnaout
Lorne J. Gula
Danna A. Spears
Peter Leong-Sit
Qiuju Li
Wadea Tarhuni
Sven Reischauer
Vijay S. Chauhan
Matthew Borkovich
Shaheen Uppal
Arnon Adler
Shaun R. Coughlin
Didier Y. R. Stainier
Michael H. Gollob
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
description Here, Michael Gollob and colleagues perform a whole exome sequencing study to identify a mutation in the atrial-specific myosin light chain gene MYL4 in a small family with autosomal dominant familial atrial fibrillation. They also test the functionality of this MYL4mutation in zebrafish cardiac function and recapitulate disease-related phenotypes.
format article
author Nathan Orr
Rima Arnaout
Lorne J. Gula
Danna A. Spears
Peter Leong-Sit
Qiuju Li
Wadea Tarhuni
Sven Reischauer
Vijay S. Chauhan
Matthew Borkovich
Shaheen Uppal
Arnon Adler
Shaun R. Coughlin
Didier Y. R. Stainier
Michael H. Gollob
author_facet Nathan Orr
Rima Arnaout
Lorne J. Gula
Danna A. Spears
Peter Leong-Sit
Qiuju Li
Wadea Tarhuni
Sven Reischauer
Vijay S. Chauhan
Matthew Borkovich
Shaheen Uppal
Arnon Adler
Shaun R. Coughlin
Didier Y. R. Stainier
Michael H. Gollob
author_sort Nathan Orr
title A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
title_short A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
title_full A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
title_fullStr A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
title_full_unstemmed A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
title_sort mutation in the atrial-specific myosin light chain gene (myl4) causes familial atrial fibrillation
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/3cbe2796738e4c49b3e6beec3f1f88fe
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