APA (7th ed.) Citation

Blanc, A., Bonnet, C., Wandzel, M., Roth, V., Duffourd, Y., Safraou, H., . . . Lambert, L. (2024). Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome. American Journal of Medical Genetics. Part A, 194(9), 1. https://doi.org/10.1002/ajmg.a.63642

Chicago Style (17th ed.) Citation

Blanc, Albin, et al. "Patient with a Heterozygous Pathogenic Variant in CSNK2A1 Gene: A New Case to Update the Okur–Chung Neurodevelopmental Syndrome." American Journal of Medical Genetics. Part A 194, no. 9 (2024): 1. https://doi.org/10.1002/ajmg.a.63642.

MLA (9th ed.) Citation

Blanc, Albin, et al. "Patient with a Heterozygous Pathogenic Variant in CSNK2A1 Gene: A New Case to Update the Okur–Chung Neurodevelopmental Syndrome." American Journal of Medical Genetics. Part A, vol. 194, no. 9, 2024, p. 1, https://doi.org/10.1002/ajmg.a.63642.