A de novo KCNA3 and an inherited KCNQ3 missense variant causing a developmental and epileptic encephalopathy, intellectual disability, and behavioral anomalies

Neurogenetics 2026

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Authors: Enrica Marchionni, Vito Luigi Colona, Emanuele Agolini, Michela Murdocca, Monia Russo, Maria Stellato, Valeria Latini, Elena Campione, Anna Maria Nardone, Paola Spitalieri, Luigi Mazzone, Antonio Novelli
+2 more Federica Carla Sangiuolo, Giuseppe Novelli
DOI: 10.1007/s10048-026-00879-2
Cited by: 0
References: 24

Fields of Study & Subjects

Ion channel regulation and function Epilepsy research and treatment Genetics and Neurodevelopmental Disorders

Publication details

Journal / source
Neurogenetics
Volume
27
Issue
1
Pages
11–11
Publication date
30 January 2026
Language
EN