K, K., A, S., Y, N., J, O., UH, M. H., M, K., . . . H, S. (2026). Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder. European journal of human genetics : EJHG. https://doi.org/10.1038/s41431-026-02151-5
Chicago Style (17th ed.) CitationK, Komatsu, et al. "Hemizygous Loss-of-function Variants of EIF1AX Are Associated with a Syndromic Neurodevelopmental Disorder." European Journal of Human Genetics : EJHG 2026. https://doi.org/10.1038/s41431-026-02151-5.
MLA (9th ed.) CitationK, Komatsu, et al. "Hemizygous Loss-of-function Variants of EIF1AX Are Associated with a Syndromic Neurodevelopmental Disorder." European Journal of Human Genetics : EJHG, 2026, https://doi.org/10.1038/s41431-026-02151-5.
Warning: These citations may not always be 100% accurate.
