Sykora et al., 2011 - Google Patents
Aprataxin localizes to mitochondria and preserves mitochondrial functionSykora et al., 2011
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- 14345992564367453767
- Author
- Sykora P
- Croteau D
- Bohr V
- Wilson III D
- Publication year
- Publication venue
- Proceedings of the National Academy of Sciences
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Snippet
Ataxia with oculomotor apraxia 1 is caused by mutation in the APTX gene, which encodes the DNA strand-break repair protein aprataxin. Aprataxin exhibits homology to the histidine triad superfamily of nucleotide hydrolases and transferases and removes 5′-adenylate …
- 101700004737 APTX 0 title abstract description 154
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