RG, L., JM, O., L, P., T, W., ML, F., J, Z., . . . P, B. (2025). RNA sequencing provides functional insights and diagnostic resolution in previously unsolved rare disease cases. BMC medical genomics, 18(1), 182. https://doi.org/10.1186/s12920-025-02227-z
Chicago Style (17th ed.) CitationRG, Lewis, et al. "RNA Sequencing Provides Functional Insights and Diagnostic Resolution in Previously Unsolved Rare Disease Cases." BMC Medical Genomics 18, no. 1 (2025): 182. https://doi.org/10.1186/s12920-025-02227-z.
MLA (9th ed.) CitationRG, Lewis, et al. "RNA Sequencing Provides Functional Insights and Diagnostic Resolution in Previously Unsolved Rare Disease Cases." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 182, https://doi.org/10.1186/s12920-025-02227-z.