Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome.
Blanc A, Bonnet C, Wandzel M, Roth V, Duffourd Y, Safraou H, Leheup B, Muller F, D Colne J, Feillet F, Schmitt E, Castro M, Savatt J, Burcheri A, Nemos C, Philippe C, Lambert L.
Blanc A, et al. Among authors: lambert l.
Am J Med Genet A. 2024 May 6:e63642. doi: 10.1002/ajmg.a.63642. Online ahead of print.
Am J Med Genet A. 2024.
PMID: 38711237