APA (7th ed.) Citation

F, J. M. D. l. T., J, P. P., & I, O. (2026). Expanding the MYCN Variant Spectrum in Feingold Syndrome Type 1: A Novel N-Terminal Missense Variant Segregating in an Affected Family. Genes, 17(5), . https://doi.org/10.3390/genes17050552

Chicago Style (17th ed.) Citation

F, Javier Mérida De la Torre, Porta Pelayo J, and Ortiz-Martín I. "Expanding the MYCN Variant Spectrum in Feingold Syndrome Type 1: A Novel N-Terminal Missense Variant Segregating in an Affected Family." Genes 17, no. 5 (2026). https://doi.org/10.3390/genes17050552.

MLA (9th ed.) Citation

F, Javier Mérida De la Torre, et al. "Expanding the MYCN Variant Spectrum in Feingold Syndrome Type 1: A Novel N-Terminal Missense Variant Segregating in an Affected Family." Genes, vol. 17, no. 5, 2026, https://doi.org/10.3390/genes17050552.