Catalytic Function of PLA2G6 Is Impaired by Mutations Associated with Infantile Neuroaxonal Dystrophy but Not Dystonia-Parkinsonism

Lignende værker

• PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy
  af: Khateeb, Shareef, et al.
  Udgivet: (2006)
• Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex
  af: Kapoor, Saketh, et al.
  Udgivet: (2016)
• Disrupted Membrane Homeostasis and Accumulation of Ubiquitinated Proteins in a Mouse Model of Infantile Neuroaxonal Dystrophy Caused by PLA2G6 Mutations
  af: Malik, Ibrahim, et al.
  Udgivet: (2008)
• Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy
  af: Polster, Brenda, et al.
  Udgivet: (2010)
• Infantile neuroaxonal dystrophy caused by PLA2G6 gene mutation in a Chinese patient: A case report
  af: Wang, Baotian, et al.
  Udgivet: (2018)