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Spinocerebellar Ataxia 15: A Phenotypic Review and Expansion
Spinocerebellar ataxia 15 (SCA15) is a clinically heterogeneous movement disorder characterized by the adult onset of slowly progressive cerebellar ataxia. ITPR1 is the SCA15 causative gene. However, despite numerous reports of genetically-confirmed SCA15, phenotypic uncertainty persists. We reviewe...
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| Veröffentlicht in: | Neurol Neurochir Pol |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5378493/ https://ncbi.nlm.nih.gov/pubmed/27908616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pjnns.2016.10.006 |
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