De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues.

MLA

Smits, Daphne J., et al. “De Novo MCM6 Variants in Neurodevelopmental Disorders: A Recognizable Phenotype Related to Zinc Binding Residues.” Human Genetics, vol. 142, no. 7, July 2023, pp. 949–64. EBSCOhost, https://doi.org/10.1007/s00439-023-02569-7.

APA

Smits, D. J., Schot, R., Popescu, C. A., Dias, K.-R., Ades, L., Briere, L. C., Sweetser, D. A., Kushima, I., Aleksic, B., Khan, S., Karageorgou, V., Ordonez, N., Sleutels, F. J. G. T., van der Kaay, D. C. M., Van Mol, C., Van Esch, H., Bertoli-Avella, A. M., Roscioli, T., & Mancini, G. M. S. (2023). De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues. Human Genetics, 142(7), 949–964. https://doi.org/10.1007/s00439-023-02569-7

Chicago

Smits, Daphne J, Rachel Schot, Cristiana A Popescu, Kerith-Rae Dias, Lesley Ades, Lauren C Briere, David A Sweetser, et al. 2023. “De Novo MCM6 Variants in Neurodevelopmental Disorders: A Recognizable Phenotype Related to Zinc Binding Residues.” Human Genetics 142 (7): 949–64. doi:10.1007/s00439-023-02569-7.