Citalopram and the KCNE1 D85N variant: a case report on the implications of a genetic modifier
Citalopram and the KCNE1 D85N variant: a case report on the implications of a genetic modifier
About this item
Full title
Citalopram and the KCNE1 D85N variant: a case report on the implications of a genetic modifier
Author / Creator
Journal title
European heart journal. Case reports, 2018, Vol.2 (4), p.yty106-yty106
Language
English
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Scope and Contents
Contents
BACKGROUNDProlongation of the QT interval on the electrocardiogram is clinically important due to the association with an increased risk of sudden cardiac death. A long QT interval may be genetically determined (congenital long QT syndrome) or be drug-induced long QT syndrome e.g. caused by pharmaceutical drugs and electrolyte imbalances. CASE SUMM...
Alternative Titles
Full title
Citalopram and the KCNE1 D85N variant: a case report on the implications of a genetic modifier
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_2215017969
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2215017969
Other Identifiers
E-ISSN
2514-2119
DOI
10.1093/ehjcr/yty106
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