A valid mouse model of AGRIN-associated congenital myasthenic syndrome

Lignende værker

• LG2 Agrin Mutation Causing Severe Congenital Myasthenic Syndrome Mimics Functional Characteristics of Non-neural (z−) Agrin
  af: Maselli, Ricardo A., et al.
  Udgivet: (2011)
• Novel SEA and LG2 Agrin mutations causing congenital Myasthenic syndrome
  af: Xi, Jianying, et al.
  Udgivet: (2017)
• Congenital myasthenic syndrome–associated agrin variants affect clustering of acetylcholine receptors in a domain-specific manner
  af: Ohkawara, Bisei, et al.
  Udgivet: (2020)
• A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation in congenital myasthenic syndrome
  af: Xing, Guanglin, et al.
  Udgivet: (2019)
• Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome
  af: Wang, Aiping, et al.
  Udgivet: (2020)