PINK1 in mitochondrial function
- PMID: 18687903
- PMCID: PMC2516263
- DOI: 10.1073/pnas.0805908105
PINK1 in mitochondrial function
Conflict of interest statement
The authors declare no conflict of interest.
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Comment on
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Loss of PINK1 causes mitochondrial functional defects and increased sensitivity to oxidative stress.Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11364-9. doi: 10.1073/pnas.0802076105. Epub 2008 Aug 7. Proc Natl Acad Sci U S A. 2008. PMID: 18687901 Free PMC article.
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- Valente EM, et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science. 2004;304:1120–1122. - PubMed
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- Kitada T, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature. 1998;392:605–608. - PubMed
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- Bonifati V, et al. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science. 2003;299:256–259. - PubMed
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