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J. M. Vance All authors

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Publications While At HealthPartners

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Journal Article
  • Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. 
  • Association study of Parkin gene polymorphisms with idiopathic Parkinson disease. 
  • Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. 
  • Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. 
  • Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. 

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