Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2
Year: 2013
Type: article
Study design: Observational Study
Source: Brain
DOI: 10.1093/brain/awt068
Authors: Elisabeth Stogmann, Eva Reinthaler, Salwa ElTawil, Mohammed A. El Etribi, Mahmoud Hemeda, Nevine El Nahhas, Ahmed M. Gaber, Amal Fouad, Sherif Edris, Anna Benet-Pages, Sebastian H. Eck, Ekaterina Pataraia, Davide Mei, Alexis Brice, Suzanne Lesage, Renzo Guerrini, Friedrich Zimprich, Tim M. Strom, Alexander Zimprich
Institutions: Medical University of Vienna, Ain Shams University, Helmholtz Munich, Institut für Humangenetik, Meyer Children's Hospital, University of Florence, Centre National de la Recherche Scientifique, Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2063466473