Published 2002
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SCN1A Gene Mutations in Severe Infantile Myoclonic Epilepsy
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Abstract
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.Files
PNB-16-28-b.pdf
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- PNB-16-28-b
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2002When the item was originally created.