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TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical feature...

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical feature...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fbd3c37951794a57a006bfdb37a6a0d0

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

About this item

Full title

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

Publisher

London: Nature Publishing Group UK

Journal title

EMBO molecular medicine, 2016-12, Vol.8 (12), p.1390-1408

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Genetic causes of many familial arrhythmia syndromes remain elusive. In this study, whole‐exome sequencing (WES) was carried out on patients from three different families that presented with life‐threatening arrhythmias and high risk of sudden cardiac death (SCD). Two French Canadian probands carried identical homozygous rare variant in
TECRL

Alternative Titles

Full title

TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_fbd3c37951794a57a006bfdb37a6a0d0

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fbd3c37951794a57a006bfdb37a6a0d0

Other Identifiers

ISSN

1757-4676

E-ISSN

1757-4684

DOI

10.15252/emmm.201505719

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