Ontology highlight
ABSTRACT:
SUBMITTER: Giansante G
PROVIDER: S-EPMC11371655 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature

Giansante Giorgia G Mazzoleni Sara S Zippo Antonio G AG Ponzoni Luisa L Ghilardi Anna A Maiellano Greta G Lewerissa Elly E van Hugte Eline E Nadif Kasri Nael N Francolini Maura M Sala Mariaelvina M Murru Luca L Bassani Silvia S Passafaro Maria M
Molecular psychiatry 20230330 6
Mutations in PCDH19 gene, which encodes protocadherin-19 (PCDH19), cause Developmental and Epileptic Encephalopathy 9 (DEE9). Heterogeneous loss of PCDH19 expression in neurons is considered a key determinant of the disorder; however, how PCDH19 mosaic expression affects neuronal network activity and circuits is largely unclear. Here, we show that the hippocampus of Pcdh19 mosaic mice is characterized by structural and functional synaptic defects and by the presence of PCDH19-negative hyperexcit ...[more]