De novo STXBP1 mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin 1A

Ehud Banne*, Tzipora Falik-Zaccai, Esther Brielle, Limor Kalfon, Hagay Ladany, Danielle Klinger, Dina Schneidman-Duhovny, Michal Linial

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Medicine & Life Sciences