KVLQT1 C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome
- 4 November 1997
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation
- Vol. 96 (9) , 2778-2781
- https://doi.org/10.1161/01.cir.96.9.2778
Abstract
Background KVLQT1, the gene encoding the α-subunit of a cardiac potassium channel, is the most common cause of the dominant form of long-QT syndrome (LQT1-type), the Romano-Ward syndrome (RWS). The...Keywords
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