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Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy.
Medina, M T; Suzuki, T; Alonso, M E; Durón, R M; Martínez-Juárez, I E; Bailey, J N; Bai, D; Inoue, Y; Yoshimura, I; Kaneko, S; Montoya, M C; Ochoa, A; Prado, A Jara; Tanaka, M; Machado-Salas, J; Fujimoto, S; Ito, M; Hamano, S; Sugita, K; Ueda, Y; Osawa, M; Oguni, H; Rubio-Donnadieu, F; Yamakawa, K; Delgado-Escueta, A V.
Affiliation
  • Medina MT; Neurology Training Program, National Autonomous University of Honduras, Tegucigalpa, Honduras.
Neurology ; 70(22 Pt 2): 2137-44, 2008 May 27.
Article in En | MEDLINE | ID: mdl-18505993
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium-Binding Proteins / Family Health / Myoclonic Epilepsy, Juvenile / Mutation Limits: Female / Humans / Male Country/Region as subject: America central / Asia / Honduras / Mexico Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium-Binding Proteins / Family Health / Myoclonic Epilepsy, Juvenile / Mutation Limits: Female / Humans / Male Country/Region as subject: America central / Asia / Honduras / Mexico Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: