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Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome.

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Bibliographic Details
Title: Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome.
Authors: Blanc, Albin1, albin.blanc@gmail.com, Bonnet, Céline2,3, Wandzel, Marion2, Roth, Virginie2, Duffourd, Yannis4,5, Safraou, Hanna4,5, Leheup, Bruno3, Muller, Florence6, D Colne, Julie7, Feillet, François3,8, Schmitt, Emmanuelle9, Castro, Matheus10,11, Savatt, Jullian12, Burcheri, Adriano13, Nemos, Christophe14,15,16,17, Philippe, Christophe4,5, Lambert, Laëtitia1,3
Source: American Journal of Medical Genetics. Part A; Sep2024, Vol. 194 Issue 9, p1-6, 6p
Database: Applied Science & Technology Source
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