Lack of mutation G209A in the α-synuclein gene in French patients with familial and sporadic Parkinson's disease

Documenti analoghi

• The role of the α-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom
  di: Warner, T, et al.
  Pubblicazione: (1998)
• Familial genes in sporadic disease: Common variants of α-Synuclein gene associate with Parkinson’s disease
  di: Ross, Owen A., et al.
  Pubblicazione: (2007)
• Macroautophagy in sporadic and the genetic form of Parkinson's disease with the A53T α-synuclein mutation
  di: Huang Yue, et al.
  Pubblicazione: (2012-01-01)
• Macroautophagy in sporadic and the genetic form of Parkinson's disease with the A53T α-synuclein mutation
  di: Huang, Yue, et al.
  Pubblicazione: (2012)
• A case of late onset sporadic Parkinson's disease with an A53T mutation in α-synuclein
  di: Michell, A, et al.
  Pubblicazione: (2005)