A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

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Botulinum toxin in masticatory muscles of the adult rat induces bone loss at the condyle and alveolar regions of the mandible associated with a bone proliferation at a muscle enthesis

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OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology

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Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction

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