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article · Ophthalmology Science

Phenotypic variations in a large family with Dominant Optic Atrophy related to a novel OPA1 deletion.

2026Open accessMohamed I University

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Research topics

  • Mitochondrial Function and Pathology
  • Glycogen Storage Diseases and Myoclonus
  • Hereditary Neurological Disorders

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DOI: 10.1016/j.xops.2026.101286

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