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Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1.
Tomlinson, Susan Elizabeth; Rajakulendran, Sanjeev; Tan, Stella Veronica; Graves, Tracey Dawn; Bamiou, Doris-Eva; Labrum, Robyn W; Burke, David; Sue, Carolyn M; Giunti, Paola; Schorge, Stephanie; Kullmann, Dimitri M; Hanna, Michael G.
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  • Tomlinson SE; MRC Centre for Neuromuscular Disease, National Hospital for Neurology and Neurosurgery, London, UK.
J Neurol Neurosurg Psychiatry ; 84(10): 1107-12, 2013 Oct.
Article in En | MEDLINE | ID: mdl-23349320
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / DNA Mutational Analysis / Myokymia / Kv1.1 Potassium Channel / Genetic Carrier Screening Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Female / Humans / Male Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2013 Document type: Article Affiliation country: Reino Unido Country of publication: Reino Unido
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / DNA Mutational Analysis / Myokymia / Kv1.1 Potassium Channel / Genetic Carrier Screening Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Female / Humans / Male Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2013 Document type: Article Affiliation country: Reino Unido Country of publication: Reino Unido