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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Asıl Yazarlar: Bohlega, Saeed A, Shinwari, Jameela M, Al Sharif, Latifa J, Khalil, Dania S, Alkhairallah, Thamer S, Al Tassan, Nada A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2011
Konular:
Research Article
Online Erişim: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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