A Chinese Pediatric cystic fibrosis patient with the
c.1624G>T, p. Gly542x / c.223C>T, p. Arg75x
genotype
- Rui Zhang
, - Yao Sun
Abstract
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
