Singla, A., Rogers, C., Touma, M., El-Najjar, Y., Colley, A., Boesch, D. J., . . . Burstein, E. (2025). CCDC22 mutations that impair COMMD binding cause attenuated 3C/Ritscher-Schinzel syndrome. BMC Medical Genomics, 18(1), 1. https://doi.org/10.1186/s12920-025-02168-7
Chicago Style (17th ed.) CitationSingla, Amika, et al. "CCDC22 Mutations That Impair COMMD Binding Cause Attenuated 3C/Ritscher-Schinzel Syndrome." BMC Medical Genomics 18, no. 1 (2025): 1. https://doi.org/10.1186/s12920-025-02168-7.
MLA (9th ed.) CitationSingla, Amika, et al. "CCDC22 Mutations That Impair COMMD Binding Cause Attenuated 3C/Ritscher-Schinzel Syndrome." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 1, https://doi.org/10.1186/s12920-025-02168-7.
Warning: These citations may not always be 100% accurate.