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5. Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

9. Dystonian patofysiologia ja hoito

19. Poikkeava kävely

22. SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population

23. ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

24. ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

29. Gut microbiota are related to Parkinson's disease and clinical phenotype

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