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Prepare a B12 with me!, Are you:, Lacking sleep, Unmotivated, Suffering with anxiety & depression, Mood swings, Have you thought about trying a B12 injection? Being low in vitamin B12 can present ...
mtDNA mitochondrial DNA, nDNA nuclear DNA, PEO progressive external ophthalmoplegia, MNGIE mitochondrial neurogastrointestinal encephalomyopathy, SANDO sensory ataxia, neuropathy, dysarthria, and ophthalmoplegia, MIRAS mitochondrial recessive ataxia syndrome, MEMSA myoclonic epilepsy myopathy sensory ataxia, MCHS myocerebrohepatopathy spectrum, IOSCA infantile-onset spinocerebellar ataxia, NARP neurogenic muscle weakness, ataxia and retinitis pigmentosa, LHON Leber hereditary optic neuropathy, ADOA autosomal dominant optic atrophy, MELAS mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, MERRF myoclonic epilepsy with ragged red fibers, MIDD maternally inherited diabetes and deafness, MLASA myopathy, lactic acidosis and sideroblastic anemia Diagnostic methodology of mitochondrial diseases Given the genetic and phenotypic heterogeneity of mitochondrial genetic disorders, accurately diagnosing these diseases remains a significant challenge
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Size:Full Size | 1.7 oz/50 ml
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