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Molecular Mechanism of DNA Deadenylation by the Neurological Disease Protein Aprataxin
The human neurological disease known as ataxia with oculomotor apraxia 1 is caused by mutations in the APTX gene that encodes Aprataxin (APTX) protein. APTX is a member of the histidine triad superfamily of nucleotide hydrolases and transferases but is distinct from other family members in that it a...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Society for Biochemistry and Molecular Biology
2008
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2662222/ https://ncbi.nlm.nih.gov/pubmed/18836178 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M807124200 |
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