Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome von 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, Savatt, Jullian, Burcheri, Adriano, Nemos, Christophe, Philippe, Christophe, Lambert, Laëtitia

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