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Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies.
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
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Epilepsy with myoclonic absence presenting with unilateral jerks: A case of 2q13 microdeletion syndrome.
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Transition issues for benign epilepsy with centrotemporal spikes, nonlesional focal epilepsy in otherwise normal children, childhood absence epilepsy, and juvenile myoclonic epilepsy.