Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34.

@article{Nemeth2000AutosomalRC,
  title={Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34.},
  author={Andrea H. Nemeth and Elena G. Bochukova and Eimear M. Dunne and Susan Mary Huson and John Elston and Mohammed A. Hannan and Mike Jackson and Caroline J. Chapman and Aileen E M Taylor},
  journal={American journal of human genetics},
  year={2000},
  volume={67 5},
  pages={1320-6}
}
Ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome [AOA]; MIM 208920) is an autosomal recessive disorder characterized by ataxia, oculomotor apraxia, and choreoathetosis. These neurological features resemble those of ataxia-telangiectasia (AT), but in AOA there are none of the extraneurological features of AT, such as immunodeficiency, neoplasia, chromosomal instability, or sensitivity to ionizing radiation. It is unclear whether these patients have a true disorder of… CONTINUE READING
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