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Developmental Aspects of Long QT Syndrome and Brugada Syndrome on the Basis of a Single SCN5A Mutation in Childhood

✍ Scribed by G.C.M. Beaufort-Krol; M.P. van den Berg; A.A.M. Wilde


Book ID
113415543
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
38 KB
Volume
14
Category
Article
ISSN
1062-1458

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The long QT syndrome (LQT) is an inherited cardiac disorder that can cause sudden cardiac death among apparently healthy young individuals due to malignant ventricular arrhythmias. LQT was found to be caused by mutations in four genes LQT1, LQT2, LQT3 and LQT5, and linkage was reported for an additi