10 results on '"Wallace, Douglas C."'
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2. Reversible optic neuropathy with OPA1 exon 5b mutation
3. Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia
4. Apolipoprotein E genotype in patients with alzheimer's disease: Implications for the risk of dementia among relatives
5. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation
6. Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain
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8. Mitochondrial oxidative phosphorylation defects in parkinson's disease
9. Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
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