loading page

A Chinese Pediatric cystic fibrosis patient with the c.1624G>T, p. Gly542x / c.223C>T, p. Arg75x genotype
  • Rui Zhang,
  • Yao Sun
Rui Zhang
Chengdu Women and Children's Central Hospital
Author Profile
Yao Sun
Children's Hospital of Nanjing Medical University

Corresponding Author:[email protected]

Author Profile


In conclusion, we present this case in order to complement CFTR gene mutations data of Chinese children with cystic fibrosis and improve clinicians' understanding of this disease in China. Besides, with the development of molecular biology technology, gene detection was expected to play an important role in the early diagnosis, early treatment, and prognosis improvement of the disease.
12 Jun 2023Submitted to Pediatric Pulmonology
12 Jun 2023Review(s) Completed, Editorial Evaluation Pending
12 Jun 2023Submission Checks Completed
12 Jun 2023Assigned to Editor
14 Jun 2023Reviewer(s) Assigned
03 Jul 2023Editorial Decision: Revise Major
13 Jul 20231st Revision Received
17 Jul 2023Review(s) Completed, Editorial Evaluation Pending
17 Jul 2023Submission Checks Completed
17 Jul 2023Assigned to Editor
17 Jul 2023Reviewer(s) Assigned
21 Aug 2023Editorial Decision: Accept