He, X., Tian, Z., Guan, H., & Zhang, S. (2022). Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China. Orphanet journal of rare diseases, 17(1), 1-16. https://doi.org/10.1186/s13023-022-02481-9
Chicago Style (17th ed.) CitationHe, Xinyue, Zhuang Tian, Hongzhi Guan, and Shuyang Zhang. "Clinical Phenotypes and Genetic Features of Hereditary Transthyretin Amyloidosis Patients in China." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 1-16. https://doi.org/10.1186/s13023-022-02481-9.
MLA (9th ed.) CitationHe, Xinyue, et al. "Clinical Phenotypes and Genetic Features of Hereditary Transthyretin Amyloidosis Patients in China." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, pp. 1-16, https://doi.org/10.1186/s13023-022-02481-9.