SK, W., A, W., CA, T., PJ, B., L, E., K, F., . . . JA, R. (2024). De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities. American journal of medical genetics. Part A, 194(1), 17. https://doi.org/10.1002/ajmg.a.63399
Chicago Style (17th ed.) CitationSK, Ward, et al. "De Novo Missense Variants in ZBTB47 Are Associated with Developmental Delays, Hypotonia, Seizures, Gait Abnormalities, and Variable Movement Abnormalities." American Journal of Medical Genetics. Part A 194, no. 1 (2024): 17. https://doi.org/10.1002/ajmg.a.63399.
MLA (9th ed.) CitationSK, Ward, et al. "De Novo Missense Variants in ZBTB47 Are Associated with Developmental Delays, Hypotonia, Seizures, Gait Abnormalities, and Variable Movement Abnormalities." American Journal of Medical Genetics. Part A, vol. 194, no. 1, 2024, p. 17, https://doi.org/10.1002/ajmg.a.63399.