Published 2003
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Journal Article
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Genetics of Severe Myoclonic Epilepsy of Infancy
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Abstract
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.Files
PNB-17-51-a.pdf
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- PNB-17-51-a
Dates
- Created
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2003When the item was originally created.