10 results on '"Procaccio, Vincent"'
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2. Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation
3. 26 Biomarkers of redox abnormalities in mitochondrial disorders and organic acidemias
4. Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity
5. A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene
6. 77 Somatic mtDNA control region mutations and their effects in down syndrome with Alzheimer dementia
7. 79 Effects of common mtDNA variants on mitochondrial function
8. 76 Biochemical study of complex i deficient patient cell lines
9. 74 Mitomaster – Analytical tool for clinical mitochondrial sequence data
10. Effects of estrogen on mitochondrial function in cerebral blood vessels: Potential mechanism for vascular protection?
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