Cite
Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8.
MLA
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, Apr. 2022, pp. 1–7. EBSCOhost, https://doi.org/10.1186/s13023-022-02306-9.
APA
Yuan, H., Wang, Q., Zeng, X., He, P., Xu, W., Guo, H., Liu, Y., & 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), 1–7. https://doi.org/10.1186/s13023-022-02306-9
Chicago
Yuan, Haiming, Qingming Wang, Xiumei Zeng, Peiqing He, Wanfang Xu, Hongmei Guo, Yanhui Liu, and Yangyang Lin. 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): 1–7. doi:10.1186/s13023-022-02306-9.