Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome. - Blanc, Albin; Bonnet, Céline; Wandzel, Marion; Roth, Virginie; Duffourd, Yannis; Safraou, Hanna; Leheup, Bruno; Muller, Florence; D Colne, Julie; Feillet, François; Schmitt, Emmanuelle; Castro, Matheus; et al. (American Journal of Medical Genetics. Part A, 2024)