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Summary Anatomy Item Literature (797) Expression Attributions Wiki
XB-ANAT-542

Papers associated with chondrocranium (and grin1)

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Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy., Lemke JR., Neurology. June 7, 2016; 86 (23): 2171-8.  

GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy., Lemke JR., Ann Neurol. January 1, 2014; 75 (1): 147-54.      

Subunit-specific mechanisms and proton sensitivity of NMDA receptor channel block., Dravid SM., J Physiol. May 15, 2007; 581 (Pt 1): 107-28.

Differential contribution of the NR1- and NR2A-subunits to the selectivity filter of recombinant NMDA receptor channels., Wollmuth LP., J Physiol. March 15, 1996; 491 ( Pt 3) 779-97.

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