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Spinocerebellar Ataxia-21 in a Turkish Child
Hereditary cerebellar ataxias are genetically heterogeneous disorders. Autosomal recessive spinocerebellar ataxia-21 (SCAR21) is a neurologic disorder characterized by the onset of cerebellar ataxia, recurrent episodes of liver failure, peripheral neuropathy, and learning disabilities. Herein, we re...
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| Izdano u: | Ann Indian Acad Neurol |
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| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Medknow Publications & Media Pvt Ltd
2018
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5909149/ https://ncbi.nlm.nih.gov/pubmed/29720801 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/aian.AIAN_415_17 |
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