The complex role of protocadherin-19 in brain function:a focus on the oxytocin system
Sara Mazzoleni
Marta Busnelli
Silvia Bassani
Abstract：Mutations in the protocadherin-19 (PCDH19) gene (Xq22.1) cause the X-linked syndrome known as developmental and epileptic encephalopathy 9 (DEE9, OMIM #300088) (Dibbens et al., 2008).
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Publication Date：2025-11-27
Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)
Pages：2( 3211-3212 )