APA (7th ed.) Citation

Yuan, H., Wang, Q., Zeng, X., He, P., Xu, W., Guo, H., . . . Lin, Y. (2022). Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8. Orphanet Journal of Rare Diseases, 17(1), 1. https://doi.org/10.1186/s13023-022-02306-9

Chicago Style (17th ed.) Citation

Yuan, Haiming, Qingming Wang, Xiumei Zeng, Peiqing He, Wanfang Xu, Hongmei Guo, Yanhui Liu, and Yangyang Lin. "Clinical and Molecular Analysis of Four Unrelated Chinese Families with Pathogenic KLHL40 Variants Causing Nemaline Myopathy 8." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 1. https://doi.org/10.1186/s13023-022-02306-9.

MLA (9th ed.) Citation

Yuan, Haiming, et al. "Clinical and Molecular Analysis of Four Unrelated Chinese Families with Pathogenic KLHL40 Variants Causing Nemaline Myopathy 8." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 1, https://doi.org/10.1186/s13023-022-02306-9.