In this review, Saul Mullen and Ingrid Scheffer review the phenotypes and animal models for epilepsies associated with SCN1A mutations. This review will finally coin the term interneuronopathy for the various diseases with SCN1A mutations and is an additional reference for Severe Infantile Multifocal Epilepsy (SIMFE) beside the 2007 Harkin paper, which is freely available online.
Ingo
This 2009 blog post has been transferred to the EuroEPINOMICS blog fromwww.epilepsygenetics.net.
Please quote this blog (APA format) as
Helbig, I. Review: SCN1A in men and mice. Retrieved [enter date], from http://www.euroepinomics.wordpress.com
Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany
