APA (7th ed.) Citation

S, W., E, Y., EM, K., N, M., A, H., Q, M., . . . WT, P. (2023). Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome. Human molecular genetics, 32(12), 2055. https://doi.org/10.1093/hmg/ddad041

Chicago Style (17th ed.) Citation

S, Wang, et al. "Genetic Modifiers Modulate Phenotypic Expression of Tafazzin Deficiency in a Mouse Model of Barth Syndrome." Human Molecular Genetics 32, no. 12 (2023): 2055. https://doi.org/10.1093/hmg/ddad041.

MLA (9th ed.) Citation

S, Wang, et al. "Genetic Modifiers Modulate Phenotypic Expression of Tafazzin Deficiency in a Mouse Model of Barth Syndrome." Human Molecular Genetics, vol. 32, no. 12, 2023, p. 2055, https://doi.org/10.1093/hmg/ddad041.