The emerging role of glycine receptor α2 subunit defects in neurodevelopmental disorders

Rare neurodevelopmental disorders (NDDs) are one of the most significant unmet challenges in healthcare due to their lifelong nature, high management costs, and recurrence within families. This review will focus on newly-emerging genetic forms of NDDs resulting from variants in the glycine receptor...

Disgrifiad llawn

Manylion Llyfryddiaeth

Prif Awduron:	Sean D. Fraser, Robert J. Harvey
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	Frontiers Media S.A. 2025-02-01
Cyfres:	Frontiers in Molecular Neuroscience
Pynciau:	autism spectrum disorder cortical neuronal migration epilepsy glycine receptor Glra2 knockout mice GlyR α2 subunit
Mynediad Ar-lein:	https://www.frontiersin.org/articles/10.3389/fnmol.2025.1550863/full
Tagiau:	Ychwanegu Tag Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!