A novel WDR45 mutation in a patient with β-propeller protein-associated neurodegeneration

Samankaltaisia teoksia

• Beta-Propeller-Protein-Associated Neurodegeneration: A Case of Mutation in WDR45
  Tekijä: Ryu, Sook Won, et al.
  Julkaistu: (2015)
• A novel WDR45 mutation in a patient with static encephalopathy of childhood with neurodegeneration in adulthood (SENDA)
  Tekijä: Ozawa, Tadashi, et al.
  Julkaistu: (2014)
• A Case of Beta-propeller Protein-associated Neurodegeneration due to a Heterozygous Deletion of WDR45
  Tekijä: Hermann, Andreas, et al.
  Julkaistu: (2017)
• Is WDR45 the missing link for ER stress-induced autophagy in beta-propeller associated neurodegeneration?
  Tekijä: Mollereau, Bertrand, et al.
  Julkaistu: (2019)
• WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype
  Tekijä: Kulikovskaja, Leonora, et al.
  Julkaistu: (2018)