FTL mutation in a Chinese pedigree with neuroferritinopathy

Lignende værker

• Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement
  af: Maciel, P., et al.
  Udgivet: (2005)
• Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
  af: Devos, David, et al.
  Udgivet: (2009)
• Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy
  af: Wen, Xiao‐Dan, et al.
  Udgivet: (2015)
• Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing
  af: Lu, Cong, et al.
  Udgivet: (2016)
• Novel homozygous PANK2 mutation identified in a consanguineous Chinese pedigree with pantothenate kinase-associated neurodegeneration
  af: Li, Yan-Fang, et al.
  Udgivet: (2016)