Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing
<p>Abstract</p> <p>Background</p> <p>Long QT syndrome (LQTS) is an inherited arrhythmic disorder characterised by prolongation of the QT interval on ECG, presence of syncope and sudden death. The symptoms in LQTS patients are highly variable, and genotype influences the...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2012-10-01
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Series: | BMC Cardiovascular Disorders |
Subjects: | |
Online Access: | http://www.biomedcentral.com/1471-2261/12/95 |