A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures
- 30 September 2005
- journal article
- case report
- Published by Elsevier in Brain & Development
- Vol. 27 (6), 424-430
- https://doi.org/10.1016/j.braindev.2004.11.005
Abstract
No abstract availableKeywords
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