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Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance.
Am J Hum Genet. 2013 Sep 5;93(3):471-81. doi: 10.1016/j.ajhg.2013.07.017. Epub 2013 Aug 29.
Am J Hum Genet. 2013.
PMID: 23993193
Free PMC article.
Monitoring mitochondrial dynamics and complex I dysfunction in neurons: implications for Parkinson's disease.
Simcox EM, Reeve A, Turnbull D.
Simcox EM, et al.
Biochem Soc Trans. 2013 Dec;41(6):1618-24. doi: 10.1042/BST20130189.
Biochem Soc Trans. 2013.
PMID: 24256264
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The impact of pathogenic mitochondrial DNA mutations on substantia nigra neurons.
Reeve A, Meagher M, Lax N, Simcox E, Hepplewhite P, Jaros E, Turnbull D.
Reeve A, et al.
J Neurosci. 2013 Jun 26;33(26):10790-801. doi: 10.1523/JNEUROSCI.3525-12.2013.
J Neurosci. 2013.
PMID: 23804100
Free PMC article.
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Aggregated α-synuclein and complex I deficiency: exploration of their relationship in differentiated neurons.
Reeve AK, Ludtmann MH, Angelova PR, Simcox EM, Horrocks MH, Klenerman D, Gandhi S, Turnbull DM, Abramov AY.
Reeve AK, et al. Among authors: simcox em.
Cell Death Dis. 2015 Jul 16;6(7):e1820. doi: 10.1038/cddis.2015.166.
Cell Death Dis. 2015.
PMID: 26181201
Free PMC article.
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Ageing and Parkinson's disease: why is advancing age the biggest risk factor?
Reeve A, Simcox E, Turnbull D.
Reeve A, et al.
Ageing Res Rev. 2014 Mar;14(100):19-30. doi: 10.1016/j.arr.2014.01.004. Epub 2014 Feb 3.
Ageing Res Rev. 2014.
PMID: 24503004
Free PMC article.
Review.
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