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

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B. (2023)

First Author: Brock S
Attributed to:  The Wales Genomic Medicine Centre funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2021-107971

PubMed Identifier: 35393335

Publication URI: http://europepmc.org/abstract/MED/35393335

Type: Journal Article/Review

Volume: 60

Parent Publication: Journal of medical genetics

Issue: 2

ISSN: 0022-2593