Early clinical features in Dravet syndrome patients with and without SCN1A mutations

Author:

Petrelli Cristina,Passamonti Claudia,Cesaroni Elisabetta,Mei Davide,Guerrini Renzo,Zamponi Nelia,Provinciali Leandro

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference35 articles.

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3. Early development in Dravet syndrome; visual function impairment precedes cognitive decline;Chieffo;Epilepsy Res.,2010

4. De novo SCN1A mutations are a major cause of severe mioclonic epilepsy of infancy;Claes;Hum. Mutat.,2003

5. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am. J. Hum. Genet.,2001

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