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Scientists test new gene therapy for vision loss from a mitochondrial disease | National Institutes of Health (NIH)
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Nuclear expression of mitochondrial ND4 leads to the protein assembling in complex I and prevents optic atrophy and visual loss: Molecular Therapy - Methods & Clinical Development
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Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome | Journal of Human Genetics
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Nuclear expression of mitochondrial ND4 leads to the protein assembling in complex I and prevents optic atrophy and visual loss - ScienceDirect
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