1. OPA1: How much do we know to approach therapy?
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2. Mitochondrial dysfunction caused by novel ATAD3A mutations
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3. Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches
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4. Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants
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5. Mitochondrial Retinopathies
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6. Leigh-like neuroimaging features associated with new biallelic mutations in OPA1
   Anna Rubegni et al, 2017, European Journal of Paediatric Neurology CrossRef
7. Biallelic Optic Atrophy 1 (OPA1) Related Disorder—Case Report and Literature Review
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8. Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations
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9. Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics
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10. Leigh-like syndrome due to OPA1 mutations
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11. High-glucose Induced Mitochondrial Dynamics Disorder of Spinal Cord Neurons in Diabetic Rats and its Effect on Mitochondrial Spatial Distribution
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12. Compound Heterozygous Mutations of SACS in a Korean Cohort Study of Charcot-Marie-Tooth Disease Concurrent Cerebellar Ataxia and Spasticity
    Byung Kwon Pi et al, 2024, International Journal of Molecular Sciences CrossRef
13. Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct OPA1 mutations and clinical pathologies
    Katherine A. Pohl et al, 2023, Frontiers in Genetics CrossRef
14. Systematic review of autosomal recessive ataxias and proposal for a classification
    Marie Beaudin et al, 2017, Cerebellum & Ataxias CrossRef
15. Mitochondrial disorders of the retinal ganglion cells and the optic nerve
    Josef Finsterer et al, 2018, Mitochondrion CrossRef