APA

Stogmann E., Reinthaler E., Eltawil S., El Etribi M. A., Hemeda M., El Nahhas N., Gaber A. M., Fouad A., Edris S., Benet-Pages A., Eck S. H., Pataraia E., Mei D., Brice A., Lesage S., Guerrini R., Zimprich F., Strom T. M. & Zimprich A. (20130530). Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. : Brain : a journal of neurology.

Chicago

Stogmann Elisabeth, Reinthaler Eva, Eltawil Salwa, El Etribi Mohammed A, Hemeda Mahmoud, El Nahhas Nevine, Gaber Ahmed M, Fouad Amal, Edris Sherif, Benet-Pages Anna, Eck Sebastian H, Pataraia Ekaterina, Mei Davide, Brice Alexis, Lesage Suzanne, Guerrini Renzo, Zimprich Friedrich, Strom Tim M and Zimprich Alexander. 20130530. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. : Brain : a journal of neurology.

Harvard

Stogmann E., Reinthaler E., Eltawil S., El Etribi M. A., Hemeda M., El Nahhas N., Gaber A. M., Fouad A., Edris S., Benet-Pages A., Eck S. H., Pataraia E., Mei D., Brice A., Lesage S., Guerrini R., Zimprich F., Strom T. M. and Zimprich A. (20130530). Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. : Brain : a journal of neurology.

MLA

Stogmann Elisabeth, Reinthaler Eva, Eltawil Salwa, El Etribi Mohammed A, Hemeda Mahmoud, El Nahhas Nevine, Gaber Ahmed M, Fouad Amal, Edris Sherif, Benet-Pages Anna, Eck Sebastian H, Pataraia Ekaterina, Mei Davide, Brice Alexis, Lesage Suzanne, Guerrini Renzo, Zimprich Friedrich, Strom Tim M and Zimprich Alexander. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. : Brain : a journal of neurology. 20130530.