Title: Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
Abstract: Background: Congenital long QT syndrome (LQTS) is a primary cardiac channelopathy. Over 300 mutations have been identified in 5 genes encoding key ion channel subunits. Until the recent release of the commercial clinical genetic test, LQTS genetic testing has been performed in research laboratories over the past decade.
Publication Year: 2005
Publication Date: 2005-05-01
Language: en
Type: article
Indexed In: ['crossref']
Access and Citation
Cited By Count: 16
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