Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies

Nathan L. Absalom, Vivian W.Y. Liao, Katrine M.H. Johannesen, Elena Gardella, Julia Jacobs, Gaetan Lesca, Zeynep Gokce-Samar, Alexis Arzimanoglou, Shimriet Zeidler, Pasquale Striano, Pierre Meyer, Ira Benkel-Herrenbrueck, Inger Lise Mero, Jutta Rummel, Mary Chebib, Rikke S. Møller*, Philip K. Ahring*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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