Recurrent De Novo Mutations of SCN1A in Severe Myoclonic Epilepsy of Infancy
Titel:
Recurrent De Novo Mutations of SCN1A in Severe Myoclonic Epilepsy of Infancy
Auteur:
Kearney, Jennifer A. Wiste, Anna K. Stephani, Ulrich Trudeau, Michelle M. Siegel, Anne RamachandranNair, Rajesh Elterman, Roy D. Muhle, Hiltrud Reinsdorf, Juliane Shields, W. Donald Meisler, Miriam H. Escayg, Andrew