Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation Academic Article uri icon

Overview

MeSH Major

  • DNA, Mitochondrial
  • Parkinsonian Disorders
  • Point Mutation

abstract

  • These data reveal previously unsuspected clinical heterogeneity of the G11778A mutation, and suggest that an inherited mtDNA mutation can contribute to the development of adult-onset parkinsonism and multisystem degeneration.

publication date

  • November 10, 1999

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed ID

  • 10563629

Additional Document Info

start page

  • 1787

end page

  • 93

volume

  • 53

number

  • 8