De novo variants of IRF2BPL result in developmental epileptic disorder.

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Author(s): Wang, Yong¹ (AUTHOR) ; Ke, Zhongling¹ (AUTHOR); Li, Yufen² (AUTHOR); Qiu, Mingqi¹ (AUTHOR); Liu, Jing³ (AUTHOR); Yang, Zuozhen³ (AUTHOR); Wen, Shu³ (AUTHOR); Liang, Mengmeng³ (AUTHOR); Chen, Shan¹ (AUTHOR)
Source:
Orphanet Journal of Rare Diseases. 3/13/2024, Vol. 19 Issue 1, p1-9. 9p.