APA (7th ed.) Citation

AD, G., NA, K., GV, K., AM, K., VV, N., DS, Y., . . . DI, L. (2024). Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional properties of slow skeletal muscle tropomyosin γβ-heterodimer. Archives of biochemistry and biophysics, 752, 109881. https://doi.org/10.1016/j.abb.2023.109881

Chicago Style (17th ed.) Citation

AD, Gonchar, et al. "Myopathy-causing Mutation R91P in the TPM3 Gene Drastically Impairs Structural and Functional Properties of Slow Skeletal Muscle Tropomyosin γβ-heterodimer." Archives of Biochemistry and Biophysics 752 (2024): 109881. https://doi.org/10.1016/j.abb.2023.109881.

MLA (9th ed.) Citation

AD, Gonchar, et al. "Myopathy-causing Mutation R91P in the TPM3 Gene Drastically Impairs Structural and Functional Properties of Slow Skeletal Muscle Tropomyosin γβ-heterodimer." Archives of Biochemistry and Biophysics, vol. 752, 2024, p. 109881, https://doi.org/10.1016/j.abb.2023.109881.