Cite
Exons 1-3 deletion in FLCN is associated with increased risk of pneumothorax in Chinese patients with Birt-Hogg-Dubé syndrome.
MLA
Wang, Yue, et al. “Exons 1-3 Deletion in FLCN Is Associated with Increased Risk of Pneumothorax in Chinese Patients with Birt-Hogg-Dubé Syndrome.” Orphanet Journal of Rare Diseases, vol. 18, no. 1, May 2023, p. 115. EBSCOhost, https://doi.org/10.1186/s13023-023-02710-9.
APA
Wang, Y., Cai, M., Jiang, X., Lv, G., Hu, D., Zhang, G., Liu, J., Wei, W., Xiao, J., Shen, B., Ryu, J. H., & Hu, X. (2023). Exons 1-3 deletion in FLCN is associated with increased risk of pneumothorax in Chinese patients with Birt-Hogg-Dubé syndrome. Orphanet Journal of Rare Diseases, 18(1), 115. https://doi.org/10.1186/s13023-023-02710-9
Chicago
Wang, Yue, Mengru Cai, Xianliang Jiang, Guangyu Lv, Daiju Hu, Guofeng Zhang, Jinli Liu, et al. 2023. “Exons 1-3 Deletion in FLCN Is Associated with Increased Risk of Pneumothorax in Chinese Patients with Birt-Hogg-Dubé Syndrome.” Orphanet Journal of Rare Diseases 18 (1): 115. doi:10.1186/s13023-023-02710-9.