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Publications by Hiroya Rikimaru
Authors' Reply to 'Heteroplasmy of the M.3243A>G Mutation May Influence Phenotypic Heterogeneity'
Internal Medicine
Internal Medicine
Medicine
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Mitochondrial DNA M.3243A > G Heteroplasmy Affects Multiple Aging Phenotypes and Risk of Mortality
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Fear of Disease Progression in Carriers of the M.3243A > G Mutation
Orphanet Journal of Rare Diseases
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Glucose Metabolism Derangements in Adults With the MELAS M.3243A>G Mutation
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Reduced Bone Mineral Density in M.3243A > G Carriers May Be Multifactorial
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Heteroplasmy Rates of the M.14495A>G Variant in MT-ND6 May Not Predict the Phenotype of LHON
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Classification of CFTR Mutation Classes – Authors' Reply
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Contribution of the tRNAIle4317A>G Mutation to the Phenotypic Manifestation of the Deafness-Associated Mitochondrial 12S rRNA 1555A>G Mutation
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De Novo Mutation of M.3243A>G Together With M.16093T>C Associated With Atypical Clinical Features in a Pedigree With MIDD Syndrome
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Natural History of MELAS Associated With Mitochondrial DNA M.3243A>G Genotype
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