PTCD3 mutations cause Leigh-like rather than Leigh syndrome
- PMID: 30706245
- DOI: 10.1007/s10048-019-00566-5
PTCD3 mutations cause Leigh-like rather than Leigh syndrome
Comment in
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Reply to the "Letter to the Editor" from Dr. J Finsterer and colleagues.Neurogenetics. 2019 Mar;20(1):55-56. doi: 10.1007/s10048-019-00567-4. Epub 2019 Feb 21. Neurogenetics. 2019. PMID: 30788637 No abstract available.
Comment on
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Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome.Neurogenetics. 2019 Mar;20(1):9-25. doi: 10.1007/s10048-018-0561-9. Epub 2019 Jan 3. Neurogenetics. 2019. PMID: 30607703
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Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome.Neurogenetics. 2019 Mar;20(1):9-25. doi: 10.1007/s10048-018-0561-9. Epub 2019 Jan 3. Neurogenetics. 2019. PMID: 30607703
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