LAUSR

073_16776-B2 Unexpectedly High Incidence of T309I Mutation in KCNQ1 Gene Among Czech Families With Long QT Syndrome

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1 Published in 2017 at "JACC: Clinical Electrophysiology"

DOI: 10.1016/j.jacep.2017.09.050

Abstract: Mutations in up to 15 genes have been associated with long QT syndrome (LQTS), most encoding for subunits of cardiac ionic channels. In majority of cases, each family has its “own” mutation. Individuals with suspected… read more here.

Keywords: 073 16776; long syndrome; unexpectedly high; high incidence ... See more keywords