Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome
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Title
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome
Authors
Keywords
Leigh syndrome, Oxidative phosphorylation, PTCD3, Small mitoribosomal subunit, Mitochondrial translation
Journal
NEUROGENETICS
Volume -, Issue -, Pages -
Publisher
Springer Nature
Online
2019-01-04
DOI
10.1007/s10048-018-0561-9
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