APA (7th ed.) Citation

T, H., J, L., J, J., J, M., F, S., HC, A., & K, K. (2022). Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala). Human mutation, 43(9), 1224. https://doi.org/10.1002/humu.24397

Chicago Style (17th ed.) Citation

T, Holling, Lisfeld J, Johannsen J, Matschke J, Song F, Altmeppen HC, and Kutsche K. "Autosomal Dominantly Inherited Myopathy Likely Caused by the TNNT1 Variant P.(Asp65Ala)." Human Mutation 43, no. 9 (2022): 1224. https://doi.org/10.1002/humu.24397.

MLA (9th ed.) Citation

T, Holling, et al. "Autosomal Dominantly Inherited Myopathy Likely Caused by the TNNT1 Variant P.(Asp65Ala)." Human Mutation, vol. 43, no. 9, 2022, p. 1224, https://doi.org/10.1002/humu.24397.