DOI:
10.1055/s-00037682
International Journal of Epilepsy
LinksClose Window
References
Morimoto M, Mazaki E, Nishimura A. et al.
SCN1A mutation mosaicism in a family with severe myoclonic epilepsy in infancy.
Epilepsia
47 2006; 1732-1736
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.