GRIN2A
glutamate ionotropic receptor NMDA type subunit 2A
Ассоциированные заболевания
Герминативная мутация (причина)5
Rolandic epilepsy-speech dyspraxia syndromeORPHA:163721
→Self-limited epilepsy with centrotemporal spikesORPHA:1945
→Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutationORPHA:289266
→Developmental and epileptic encephalopathy with spike-wave activation in sleepORPHA:725
→Landau-Kleffner syndromeORPHA:98818
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