Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies: Revision history

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17 June 2019

18 July 2017

  • curprev 21:2721:27, 18 July 2017‎ Ycarmen1 talk contribs‎ 2,668 bytes +2,668‎ Created page with "''Fujiwara T (2006) Clinical spectrum of mutations in scn1a gene: severe myoclonic epilepsy in infancy and related epilepsies. Epilepsy Res 70 Suppl 1: S223–30.'' '''[http:..."
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