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Reply: The expanding neurological phenotype of DNM1L-related disorders
Download from doi.orgCyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy
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Download from doi.orgNeurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults
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Download from doi.orgNovel NDUFS4 gene mutation in an atypical late-onset mitochondrial form of multifocal dystonia
Download from doi.orgAutophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophy
Download from api.wiley.comIL-26 Confers Proinflammatory Properties to Extracellular DNA
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