Ocular findings of oculomotor apraxia/ataxia type 1
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,General Medicine
Reference6 articles.
1. Autosomal recessive ataxias: 20 types, and counting;Embiruçu;Arq Neuropsiquiatr,2009
2. A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization;Ferrarini;J Neurol Sci,2007
3. Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia;Aicardi;Ann Neurol,1988
4. Aprataxin, poly-ADP ribose polymerase 1 (PARP-1) and apurinic endonuclease 1 (APE1) function together to protect the genome against oxidative damage;Harris;Hum Mol Genet,2009
5. The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates;Ahel;Nature,2006
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