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2018 | 2 |
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Page 1
Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.
Mov Disord. 2018 Oct;33(10):1591-1600. doi: 10.1002/mds.64. Epub 2018 Sep 5.
Mov Disord. 2018.
PMID: 30256453
Free PMC article.
Neuronal complex I deficiency occurs throughout the Parkinson's disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage.
Flønes IH, Fernandez-Vizarra E, Lykouri M, Brakedal B, Skeie GO, Miletic H, Lilleng PK, Alves G, Tysnes OB, Haugarvoll K, Dölle C, Zeviani M, Tzoulis C.
Flønes IH, et al.
Acta Neuropathol. 2018 Mar;135(3):409-425. doi: 10.1007/s00401-017-1794-7. Epub 2017 Dec 21.
Acta Neuropathol. 2018.
PMID: 29270838
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