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Year | Number of Results |
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2010 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
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Recurrent tissue-specific mtDNA mutations are common in humans.
PLoS Genet. 2013 Nov;9(11):e1003929. doi: 10.1371/journal.pgen.1003929. Epub 2013 Nov 7.
PLoS Genet. 2013.
PMID: 24244193
Free PMC article.
Epigenetics, epidemiology and mitochondrial DNA diseases.
Chinnery PF, Elliott HR, Hudson G, Samuels DC, Relton CL.
Chinnery PF, et al.
Int J Epidemiol. 2012 Feb;41(1):177-87. doi: 10.1093/ije/dyr232. Epub 2012 Jan 28.
Int J Epidemiol. 2012.
PMID: 22287136
Free PMC article.
Review.
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OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.
Yu-Wai-Man P, Sitarz KS, Samuels DC, Griffiths PG, Reeve AK, Bindoff LA, Horvath R, Chinnery PF.
Yu-Wai-Man P, et al.
Hum Mol Genet. 2010 Aug 1;19(15):3043-52. doi: 10.1093/hmg/ddq209. Epub 2010 May 18.
Hum Mol Genet. 2010.
PMID: 20484224
Free PMC article.
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