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: | Book |
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Pediatric Neurology Briefs Publishers,
2002-04-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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