Papale LA et al. (2009). Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice. Human molecular genetics. 18 [PubMed]

See more from authors: Papale LA · Beyer B · Jones JM · Sharkey LM · Tufik S · Epstein M · Letts VA · Meisler MH · Frankel WN · Escayg A

References and models cited by this paper
References and models that cite this paper

Wimmer VC et al. (2010). Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus. The Journal of clinical investigation. 120 [PubMed]

This website requires cookies and limited processing of your personal data in order to function. By continuing to browse or otherwise use this site, you are agreeing to this use. See our Privacy policy and how to cite and terms of use.