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Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation |
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| Authors: | Martje E. van Egmond MD Corien C. Verschuuren‐Bemelmans MD Esther A. Nibbeling MSc Jan Willem J. Elting MD PhD Deborah A. Sival MD PhD Oebele F. Brouwer MD PhD Jeroen J. de Vries MD Hubertus P. Kremer MD PhD Richard J. Sinke PhD Marina A. Tijssen MD PhD Tom J. de Koning MD PhD |
| Affiliation: | 1. Department of Neurology, University of Groningen, University Medical Center Groningen, , The Netherlands;2. Department of Genetics, University of Groningen, University Medical Center Groningen, , The Netherlands;3. Department of Pediatrics, University of Groningen, University Medical Center Groningen, , The Netherlands |
| Abstract: | |
| Keywords: | Ramsay Hunt progressive myoclonus ataxia GOSR2 mutation myoclonus ataxia |