about
A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia.The bioactive protein-ligand conformation of GluN2C-selective positive allosteric modulators bound to the NMDA receptor.De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.
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description
researcher ORCID ID = 0000-0001-9723-4812
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wetenschapper
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name
Gil H Shaulsky
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Gil H Shaulsky
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Gil H Shaulsky
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type
label
Gil H Shaulsky
@ast
Gil H Shaulsky
@en
Gil H Shaulsky
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prefLabel
Gil H Shaulsky
@ast
Gil H Shaulsky
@en
Gil H Shaulsky
@nl
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0000-0001-9723-4812