Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder (2023)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2023.100922
PubMed Identifier: 37403762
Publication URI: http://europepmc.org/abstract/MED/37403762
Type: Journal Article/Review
Parent Publication: Genetics in Medicine
Issue: 11
ISSN: 1098-3600