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Year | Number of Results |
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2010 | 1 |
2013 | 1 |
2014 | 1 |
2017 | 1 |
2024 | 0 |
PubMed (cited) for id: 615898
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A Novel Potentially Causative Variant of NDUFAF7 Revealed by Mutation Screening in a Chinese Family With Pathologic Myopia.
Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):4182-4192. doi: 10.1167/iovs.16-20941.
Invest Ophthalmol Vis Sci. 2017.
PMID: 28837730
The arginine methyltransferase NDUFAF7 is essential for complex I assembly and early vertebrate embryogenesis.
Zurita Rendón O, Silva Neiva L, Sasarman F, Shoubridge EA.
Zurita Rendón O, et al.
Hum Mol Genet. 2014 Oct 1;23(19):5159-70. doi: 10.1093/hmg/ddu239. Epub 2014 May 16.
Hum Mol Genet. 2014.
PMID: 24838397
Free PMC article.
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NDUFAF7 methylates arginine 85 in the NDUFS2 subunit of human complex I.
Rhein VF, Carroll J, Ding S, Fearnley IM, Walker JE.
Rhein VF, et al.
J Biol Chem. 2013 Nov 15;288(46):33016-26. doi: 10.1074/jbc.M113.518803. Epub 2013 Oct 2.
J Biol Chem. 2013.
PMID: 24089531
Free PMC article.
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MidA is a putative methyltransferase that is required for mitochondrial complex I function.
Carilla-Latorre S, Gallardo ME, Annesley SJ, Calvo-Garrido J, Graña O, Accari SL, Smith PK, Valencia A, Garesse R, Fisher PR, Escalante R.
Carilla-Latorre S, et al.
J Cell Sci. 2010 May 15;123(Pt 10):1674-83. doi: 10.1242/jcs.066076. Epub 2010 Apr 20.
J Cell Sci. 2010.
PMID: 20406883
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