De Novo Mutations and Rare Variants Occurring in NMDA Receptors

Benzer Materyaller

• A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia
  Yazar:: Gao, Kai, ve diğerleri
  Baskı/Yayın Bilgisi: (2017)
• De Novo GRIN Variants in NMDA Receptor M2 Channel Pore-Forming Loop Are Associated with Neurological Diseases
  Yazar:: Li, Jia, ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.
  Yazar:: Kai Gao, ve diğerleri
  Baskı/Yayın Bilgisi: (2017-01-01)
• GRIN and Bear the Diverse Functional Effects of Rare NMDA Receptor Variants
  Yazar:: Weston, Matthew C.
  Baskı/Yayın Bilgisi: (2017)
• The GluN2B-Glu413Gly NMDA receptor variant arising from a de novo GRIN2B mutation promotes ligand-unbinding and domain opening
  Yazar:: Wells, Gordon, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)