De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
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- 1 June 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (6), 1327-1332
- https://doi.org/10.1086/320609
Abstract
No abstract availableKeywords
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