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ataxia with oculomotor apraxia, I & II

 

Definition: two distinct autosomal recessive ataxias of childhood onset in which oculomotor apraxia is prominent. Both ataxias are due to gene mutations, with type II linked to a gene on chromosome 9q.

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© Copyright 2018 Wolters Kluwer. All Rights Reserved. Review date: Sep 19, 2016.

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