Mutations in PLA2G6 and the riddle of Schindler disease

Ítems similars

• PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron
  per: Morgan, Neil V, et al.
  Publicat: (2006)
• PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy
  per: Khateeb, Shareef, et al.
  Publicat: (2006)
• PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease
  per: Illingworth, M.A., et al.
  Publicat: (2014)
• Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy
  per: Polster, Brenda, et al.
  Publicat: (2010)
• Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease
  per: Ferese, Rosangela, et al.
  Publicat: (2018)