Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome. (2022)
Attributed to:
Molecular and Bioinformatic support for the European Xenopus Resource Centre
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2022.05.009
PubMed Identifier: 35675825
Publication URI: http://europepmc.org/abstract/MED/35675825
Type: Journal Article/Review
Volume: 109
Parent Publication: American journal of human genetics
Issue: 7
ISSN: 0002-9297