Leigh syndrome
Author:
Publisher
Elsevier
Reference124 articles.
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2. Pediatric Leigh syndrome: neuroimaging features and genetic correlations;Alves;Ann Neurol,2020
3. Mutations in COX10 result in a defect in mitochondrial heme a biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency;Antonicka;Hum Mol Genet,2003
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