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Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia
BACKGROUND: Autosomal recessive ataxias represent a group of clinically overlapping disorders. These include ataxia with oculomotor apraxia type1 (AOA1), ataxia with oculomotor apraxia type 2 (AOA2) and ataxia-telangiectasia-like disease (ATLD). Patients are mainly characterized by cerebellar ataxia...
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| Main Authors: | , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2011
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3048493/ https://ncbi.nlm.nih.gov/pubmed/21324166 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-12-27 |
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