A, S., C, R., MJ, T., Y, E., A, C., DJ, B., . . . E, B. (2025). CCDC22 mutations that impair COMMD binding cause attenuated 3C/Ritscher-Schinzel syndrome. BMC medical genomics, 18(1), 98. https://doi.org/10.1186/s12920-025-02168-7
Chicago Style (17th ed.) CitationA, Singla, et al. "CCDC22 Mutations That Impair COMMD Binding Cause Attenuated 3C/Ritscher-Schinzel Syndrome." BMC Medical Genomics 18, no. 1 (2025): 98. https://doi.org/10.1186/s12920-025-02168-7.
MLA (9th ed.) CitationA, Singla, et al. "CCDC22 Mutations That Impair COMMD Binding Cause Attenuated 3C/Ritscher-Schinzel Syndrome." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 98, https://doi.org/10.1186/s12920-025-02168-7.
Warning: These citations may not always be 100% accurate.