De Novo Mutations and Rare Variants Occurring in NMDA Receptors

समान संसाधन

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