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Tolmacheva ER, Shubina J, Kochetkova TO, Ushakova LV, Bokerija EL, Vasiliev GS, Mikhaylovskaya GV, Atapina EE, Zaretskaya NV, Sukhikh GT, et al. CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes. 2023; 14(6):1177. https://doi.org/10.3390/genes14061177

Tolmacheva, Ekaterina R., Jekaterina Shubina, Taisiya O. Kochetkova, Lubov’ V. Ushakova, Ekaterina L. Bokerija, Grigory S. Vasiliev, Galina V. Mikhaylovskaya, Ekaterina E. Atapina, Nadezhda V. Zaretskaya, Gennady T. Sukhikh, and et al. 2023. "CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report" Genes 14, no. 6: 1177. https://doi.org/10.3390/genes14061177

Tolmacheva, E. R., Shubina, J., Kochetkova, T. O., Ushakova, L. V., Bokerija, E. L., Vasiliev, G. S., Mikhaylovskaya, G. V., Atapina, E. E., Zaretskaya, N. V., Sukhikh, G. T., Rebrikov, D. V., & Trofimov, D. Y. (2023). CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes, 14(6), 1177. https://doi.org/10.3390/genes14061177