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Spinocerebellar Ataxia Type 10: Frequency of epilepsy in a large sample of Brazilian patients
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder caused by an ATTCT repeat intronic expansion in the SCA10 gene. SCA 10 has been reported in Mexican, Brazilian, Argentinean and Venezuelan families. Its phenotype is overall characterized by cerebellar ataxia and epilepsy. Inte...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3000879/ https://ncbi.nlm.nih.gov/pubmed/20818609 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.23324 |
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