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Two de novo GluN2B mutations affect multiple NMDAR-functions and instigate severe pediatric encephalopathy
Shai Kellner, Abeer Abbasi, Ido Carmi, Ronit Heinrich, Tali Garin-Shkolnik, Tova Hershkovitz, Moshe Giladi, Yoni Haitin, Katrine M. Johannesen, Rikke Steensbjerre Møller, Shai Berlin*
*Corresponding author af dette arbejde
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(Scopus)