Genetics of Severe Myoclonic Epilepsy of Infancy
DOI:
https://doi.org/10.15844/pedneurbriefs-17-7-3Keywords:
Severe Myoclonic Epilepsy of Infancy, Asymptomatic, SCN1A MutationsAbstract
The role of SCN1A gene mutations in the etiology of severe myoclonic epilepsy of infancy (SMEI) was investigated in 93 patients followed at the Hopital Saint Vincent de Paul, Paris, and other centers in France and Italy.Published
2003-07-01
Issue
Section
Seizure Disorders
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Copyright (c) 2003 The Author(s)
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