Familial Parkinsonism and early onset Parkinson's disease in a Brazilian Movement Disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1 and LRRK2 mutations

Lignende værker

• Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2
  af: Bras, Jose, et al.
  Udgivet: (2008)
• Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3
  af: Okubadejo, Njideka, et al.
  Udgivet: (2008)
• Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson’s Disease
  af: Oczkowska, Anna, et al.
  Udgivet: (2013)
• Low prevalence of PANK2 mutations in Brazilian patients with early onset generalised dystonia and basal ganglia abnormalities on MRI
  af: Camargos, S T, et al.
  Udgivet: (2010)
• Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early‐onset Parkinson’s disease
  af: Nguyen Dang Ton, et al.
  Udgivet: (2020-10-01)