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Cognitive Functions in Ataxia with Oculomotor Apraxia Type 2
Background: Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by cerebellar atrophy, peripheral neuropathy, oculomotor apraxia, and elevated serum alpha-fetoprotein (AFP) levels. The disease is caused by a recessive mutation in the senataxin gene. Since it is a very rare cerebellar disor...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Research Foundation
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3449493/ https://ncbi.nlm.nih.gov/pubmed/23015802 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2012.00125 |
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