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See Latest ArticlesNeonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
Epilepsia, 11/10/09
Heron SE et al. – A previously described mutation and a known rare variant were found in the LQTS–associated genes SCN5A and KCNE2. Both are expressed in the brain, and although mutations have not been associated with epilepsy, the authors propose a pathophysiologic mechanism by which the combination of molecular changes may cause seizures.
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