📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! Tell us what works, what doesn't, and how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community. Please send your feedback to gateway@ukri.org by 11 August 2025.

Impaired neurogenesis and neural progenitor fate choice in a human stem cell model of SETBP1 disorder. (2023)

First Author: Cardo LF

Attributed to: MRC Centre for Neuropsychiatric Genetics and Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13229-023-00540-x

PubMed Identifier: 36805818

Publication URI: http://europepmc.org/abstract/MED/36805818

Type: Journal Article/Review

Volume: 14

Parent Publication: Molecular autism

Issue: 1