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Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria
Spinocerebellar ataxia type-7 (SCA7) is a cytosine-adenine-guanine (CAG) repeat polyglutamine disorder characterized by progressive degeneration of the cerebellum, brainstem, spinal cord, and retina. Clinical features include progressive ataxia, visual loss, pyramidal weakness, sensory impairment, a...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Ann Afr Med |
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| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
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Medknow Publications & Media Pvt Ltd
2016
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5402823/ https://ncbi.nlm.nih.gov/pubmed/27044733 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1596-3519.176205 |
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