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.;
et al. CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes 2023, 14, 1177.
https://doi.org/10.3390/genes14061177
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
