Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4

por Beyer, Barbara, Deleuze, Charlotte, Letts, Verity A., Mahaffey, Connie L., Boumil, Rebecca M., Lew, Timothy A., Huguenard, John R., Frankel, Wayne N.
Publicado 2008

A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice

por Boumil, Rebecca M., Letts, Verity A., Roberts, Monica C., Lenz, Christine, Mahaffey, Connie L., Zhang, Zhong-wei, Moser, Tobias, Frankel, Wayne N.
Publicado 2010

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy

por Asinof, Samuel K., Sukoff Rizzo, Stacey J., Buckley, Alexandra R., Beyer, Barbara J., Letts, Verity A., Frankel, Wayne N., Boumil, Rebecca M.
Publicado 2015

Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis

por Dhindsa, Ryan S., Bradrick, Shelton S., Yao, Xiaodi, Heinzen, Erin L., Petrovski, Slave, Krueger, Brian J., Johnson, Michael R., Frankel, Wayne N., Petrou, Steven, Boumil, Rebecca M., Goldstein, David B.
Publicado 2015