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OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 11, p. N.PAG, doi. 10.15252/emmm.201809060
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- Article
Tissue-specific modulation of mitochondrial DNA segregation by a defect in mitochondrial division.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 4, p. 706, doi. 10.1093/hmg/ddv508
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- Publication type:
- Article
Quantitative Changes in Gimap3 and Gimap5 Expression Modify Mitochondrial DNA Segregation in Mice.
- Published in:
- Genetics, 2015, v. 200, n. 1, p. 221, doi. 10.1534/genetics.115.175596
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- Article
RNA modification landscape of the human mitochondrial tRNA<sup>Lys</sup> regulates protein synthesis.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06471-z
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- Article