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

類似資料

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