Aprataxin localizes to mitochondria and preserves mitochondrial function

Medicine & Life Sciences

• Amino Acid Sequence 29%
• Autosomal recessive 1 Spinocerebellar ataxia 57%
• Brain 15%
• Cerebellum 29%
• Citrate (si)-Synthase 42%
• DNA 35%
• DNA Breaks 39%
• DNA Damage 27%
• Early-onset ataxia with oculomotor apraxia and hypoalbuminemia 60%
• Enzymes 17%
• Genes 12%
• Histidine 35%
• Hydrolases 37%
• Ligation 27%
• Mitochondria 78%
• Mitochondrial DNA 100%
• Mutation 17%
• Neuroblastoma 31%
• Nucleotides 25%
• Protein Isoforms 25%
• Proteins 11%
• Skeletal Muscle 25%
• Skeletal Myoblasts 47%
• Transferases 32%