Alpha-synuclein pathology and Parkinsonism associated withPOLG1mutations and multiple mitochondrial DNA deletions
Author:
Publisher
Wiley
Subject
Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2008.00981.x/fullpdf
Reference14 articles.
1. Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age;Corral-Debrinski;Nat Genet,1992
2. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease;Bender;Nat Genet,2006
3. Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence?;Melberg;Acta Neuropathol (Berl),2005
4. Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons;Kraytsberg;Nat Genet,2006
5. Mitochondrial DNA polymerase-γ and human disease;Hudson;Human Mol Genet,2006
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