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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...
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| Publicado no: | Ann Afr Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acesso em linha: | 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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