Genetic & Genomic MedicinemedRxivPreprint
Gain and loss of function variants in EZH1 disrupt neurogenesis timing and cause overlapping neurodevelopmental disorders
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Author
Consejo Superior de Investigaciones CientíficasORCID 0000-0003-0173-0964Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
2 papers
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Gwenvaël Le Dréau, René Escalona, Raquel Fueyo…·Elisa Martı́
The paper shows E proteins differentially cooperate with proneural bHLH transcription factors to sharpen neurogenesis by acting on specific DNA motifs.