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Ramsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation.
van Egmond, Martje E; Verschuuren-Bemelmans, Corien C; Nibbeling, Esther A; Elting, Jan Willem J; Sival, Deborah A; Brouwer, Oebele F; de Vries, Jeroen J; Kremer, Hubertus P; Sinke, Richard J; Tijssen, Marina A; de Koning, Tom J.
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  • van Egmond ME; Department of Neurology, University of Groningen, University Medical Center Groningen, The Netherlands.
Mov Disord ; 29(1): 139-43, 2014 Jan.
Article in En | MEDLINE | ID: mdl-24458321
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myoclonic Cerebellar Dyssynergia / Muscle, Skeletal / Qb-SNARE Proteins / Mutation Limits: Adult / Child / Humans / Male Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2014 Document type: Article Affiliation country: Netherlands
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myoclonic Cerebellar Dyssynergia / Muscle, Skeletal / Qb-SNARE Proteins / Mutation Limits: Adult / Child / Humans / Male Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2014 Document type: Article Affiliation country: Netherlands