DOI:
10.1055/s-00037682
International Journal of Epilepsy
LinksClose Window
References
Marini C, Mei D, Helen Cross J, Guerrini R.
Mosaic SCN1A mutation in familial severe myoclonic epilepsy of infancy.
Epilepsia
47 2006; 1737-1740
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.