| For: | Wang YQ, Hao CL, Jiang WJ, Lu YH, Sun HQ, Gao CY, Wu M. c.753_754delAG, a novel CFTR mutation found in a Chinese patient with cystic fibrosis: A case report and review of the literature. World J Clin Cases 2019; 7(15): 2110-2119 [PMID: 31423445 DOI: 10.12998/wjcc.v7.i15.2110] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v7/i15/2110.htm |
| Number | Citing Articles |
| 1 |
Yuxiao Sun, Junbao Du, Lifen Gong, Jialiang Wang, Jing Zhang, Yaqin Xu, Lei Wang, Ziwei Zhang, Hang Cheng. Current Status and the Need for CFTR Modulator Therapy in Cystic Fibrosis Patients in Mainland China: A Case Report and Literature Review. Pediatric Pulmonology 2026; 61(4) doi: 10.1002/ppul.71590
|
| 2 |
Khadijat Abubakar Bobbo, Umar Ahmad, De-Ming Chau, Norshariza Nordin, Syahril Abdullah. A comprehensive review of cystic fibrosis in Africa and Asia. Saudi Journal of Biological Sciences 2023; 30(7): 103685 doi: 10.1016/j.sjbs.2023.103685
|
| 3 |
Zixin Wang, Guizhi Zuo, Ye Shi, Yinghao Zhao, Xue Fan, Xia Hou, Qingtian Wu. Distinct CFTR Mutation Spectrum and Atypical Clinical Presentations in Chinese Patients with Cystic Fibrosis. International Journal of Molecular Sciences 2026; 27(6): 2770 doi: 10.3390/ijms27062770
|
| 4 |
Ji-Peng Duan. Cystic fibrosis caused by homozygous CFTR gene mutation leading to pulmonary involvement: a case report. American Journal of Translational Research 2025; 17(5): 3813 doi: 10.62347/ENOM2926
|
| 5 |
Yuelin Shen, Xiaolei Tang, Qionghua Chen, Hui Xu, Hui Liu, Jinrong Liu, Haiming Yang, Huimin Li, Shunying Zhao. Genetic spectrum of Chinese children with cystic fibrosis: comprehensive data analysis from the main referral centre in China. Journal of Medical Genetics 2023; 60(3): 310 doi: 10.1136/jmg-2022-108501
|