The Ala53Thr Mutation in the α‐Synuclein Gene in an Indian Patient with Young‐Onset Parkinson's Disease

Lignende værker

• Human α-synuclein-harboring familial Parkinson's disease-linked Ala-53 → Thr mutation causes neurodegenerative disease with α-synuclein aggregation in transgenic mice
  af: Lee, Michael K., et al.
  Udgivet: (2002)
• Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein.
  af: Athanassiadou, A, et al.
  Udgivet: (1999)
• Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family
  af: Kojovic, Maja, et al.
  Udgivet: (2012)
• A case of late onset sporadic Parkinson's disease with an A53T mutation in α-synuclein
  af: Michell, A, et al.
  Udgivet: (2005)
• Early-Onset of Transthyretin Amyloidosis in a Young Afro-Caribbean Woman With Thr60Ala Mutation
  af: Keppel, Stormy C., et al.
  Udgivet: (2020)