Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies

Authors


Dr Alfredo Orrico
Molecular Medicine
Azienda Ospedaliera Universitaria Senese
“S. Maria alle Scotte” Hospital
53100 Siena
Italy
Tel.:/Fax: +39 0577 586264
e-mail: a.orrico@ao-siena.toscana.it

No abstract is available for this article.

Ancillary