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Mutations In Rare Ataxia Genes Are Uncommon Causes of Sporadic Cerebellar Ataxia
BACKGROUND: Sporadic-onset ataxia is common in a tertiary care setting but a significant percentage remains unidentified despite extensive evaluation. Rare genetic ataxias, reported only in specific populations or families, may contribute to a percentage of sporadic ataxia. METHODS: Patients with ad...
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| Glavni autori: | , , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2012
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3323119/ https://ncbi.nlm.nih.gov/pubmed/22287014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.24064 |
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