APA (7th ed.) Citation

M, M., A, M., S, S., S, C., I, A., G, G., . . . A, A. (2025). A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome. Clinical genetics, 108(5), 576. https://doi.org/10.1111/cge.14763

Chicago Style (17th ed.) Citation

M, Mingoia, et al. "A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome." Clinical Genetics 108, no. 5 (2025): 576. https://doi.org/10.1111/cge.14763.

MLA (9th ed.) Citation

M, Mingoia, et al. "A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome." Clinical Genetics, vol. 108, no. 5, 2025, p. 576, https://doi.org/10.1111/cge.14763.

Warning: These citations may not always be 100% accurate.