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Deficiency of the histone lysine demethylase KDM5B causes autism-like phenotypes via increased NMDAR signalling (2024)

First Author: Pérez-Sisqués L

Attributed to: ICF: Epigenomics Rare Diseases Node funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2024.05.28.596232

Publication URI: http://dx.doi.org/10.1101/2024.05.28.596232

Type: Preprint