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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3cbe2796738e4c49b3e6beec3f1f88fe

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

About this item

Full title

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

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2016-04, Vol.7 (1), p.11303-11303, Article 11303

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Atrial fibrillation (AF), the most common arrhythmia, is a growing epidemic with substantial morbidity and economic burden. Mechanisms underlying vulnerability to AF remain poorly understood, which contributes to the current lack of highly effective therapies. Recognizing mechanistic subtypes of AF may guide an individualized approach to patient ma...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3cbe2796738e4c49b3e6beec3f1f88fe

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3cbe2796738e4c49b3e6beec3f1f88fe

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/ncomms11303

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