Tani, H., Mito, T., Velagapudi, V., Ishikawa, K., Umehara, M., Nakada, K., . . . Hayashi, J. (2019). Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders. Scientific reports, 9(1), 16054-11. https://doi.org/10.1038/s41598-019-52372-6
Chicago Style (17th ed.) CitationTani, Haruna, Takayuki Mito, Vidya Velagapudi, Kaori Ishikawa, Moe Umehara, Kazuto Nakada, Anu Suomalainen, and Jun-Ichi Hayashi. "Disruption of the Mouse Shmt2 Gene Confers Embryonic Anaemia via Foetal Liver-specific Metabolomic Disorders." Scientific Reports 9, no. 1 (2019): 16054-11. https://doi.org/10.1038/s41598-019-52372-6.
MLA (9th ed.) CitationTani, Haruna, et al. "Disruption of the Mouse Shmt2 Gene Confers Embryonic Anaemia via Foetal Liver-specific Metabolomic Disorders." Scientific Reports, vol. 9, no. 1, 2019, pp. 16054-11, https://doi.org/10.1038/s41598-019-52372-6.