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A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes

A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_09050635e6e84eea9fe02cd858901af7

A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes

About this item

Full title

A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2021-03, Vol.11 (1), p.5243-5243, Article 5243

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Idiopathic ventricular fibrillation (IVF) causes sudden death in young adult patients without structural or ischemic heart disease. Most IVF cases are sporadic and some patients present with short-coupled torsade de pointes, the genetics of which are poorly understood. A man who had a first syncope at the age of 35 presented with frequent short-cou...

Alternative Titles

Full title

A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_09050635e6e84eea9fe02cd858901af7

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_09050635e6e84eea9fe02cd858901af7

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-021-84373-9

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