| 1 | BAFME5, CNTN2 |
| Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. | |
| Stogmann E, Reinthaler E, Eltawil S, El Etribi MA, Hemeda M, El Nahhas N, Gaber AM, Fouad A, Edris S, Benet-Pages A, Eck SH, Pataraia E, Mei D, Brice A, Lesage S, Guerrini R, Zimprich F, Strom TM, Zimprich A. | |
| Brain 136(Pt 4):1155-60. doi: 10.1093/brain/awt068. Epub 2013 Mar 21. 2013 | |