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Lack of aprataxin impairs mitochondrial functions via downregulation of the APE1/NRF1/NRF2 pathway.
Hum Mol Genet. 2015 Aug 15;24(16):4516-29. doi: 10.1093/hmg/ddv183. Epub 2015 May 14.
Hum Mol Genet. 2015.
PMID: 25976310
Free PMC article.
The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene.
Luna-Sánchez M, Díaz-Casado E, Barca E, Tejada MÁ, Montilla-García Á, Cobos EJ, Escames G, Acuña-Castroviejo D, Quinzii CM, López LC.
Luna-Sánchez M, et al.
EMBO Mol Med. 2015 May;7(5):670-87. doi: 10.15252/emmm.201404632.
EMBO Mol Med. 2015.
PMID: 25802402
Free PMC article.
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