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