SCN1A Gene Mutations in Severe Infantile Myoclonic Epilepsy
Ten novel mutations of SCN1A were found in in a pair of monozygotic twins and 12 unrelated Japanese infants with severe myoclonic epilepsy in infancy (SMEI) examined at the Brain Science Institute, Saitama; and National Epilepsy Center, Shizuoko, Japan.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2002-04-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/1641 |