Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia

Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia

<p>Abstract</p> <p>Background</p> <p>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)....

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Bibliographic Details
Main Authors: Alkhairallah Thamer S, Khalil Dania S, Al Sharif Latifa J, Shinwari Jameela M, Bohlega Saeed A, Al Tassan Nada A
Format: Article
Language:English
Published: BMC 2011-02-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/12/27

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http://www.biomedcentral.com/1471-2350/12/27

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