A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A (Q58417059)
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scientific article published on 01 September 2006
Language | Label | Description | Also known as |
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English | A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A |
scientific article published on 01 September 2006 |
Statements
A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A (English)
Mulley JC
Nelson P
Guerrero S
Dibbens L
Iona X
Harkin L
Schouten J
1 September 2006