Author(s): Sitarz KS, Chinnery PF, Yu-Wai-Man P
Keywords: Dominant optic atrophy Haplogroup Hereditary spastic paraplegia, Heteroplasmy Idebenone Leber hereditary optic neuropathy Mitochondrial DNA OPA1 MUTATIONS CLINICAL EXPRESSION DNA DISEASE NEUROPATHY ATROPHY FUSION GENE DYSFUNCTION IDENTIFICATION DEFICIENCY
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Professor Patrick Chinnery
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