A Chinese pediatric cystic fibrosis patient with the c.1624G>T, p. Gly542x/c.223C>T, p. Arg75x genotype-Reference-Cited by-同舟云学术

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A Chinese pediatric cystic fibrosis patient with the c.1624G>T, p. Gly542x/c.223C>T, p. Arg75x genotype

Published:2023-09-06 Issue:12 Volume:58 Page:3619-3621
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatric Pulmonology

Author:

Zhang Rui¹^ORCID,Sun Yao²

Affiliation:

1. Department of Pharmacy, Chengdu Women's and Children's Central Hospital, School of Medicine University of Electronic Science and Technology of China Chengdu China

2. Department of Pharmacy Children's Hospital of Nanjing Medical University Nanjing China

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.26662

Reference6 articles.

1. A systematic review of the clinical and genetic characteristics of Chinese patients with cystic fibrosis

2. Cystic fibrosis

3. Ataluren and similar compounds (specific therapies for premature termination codon class I mutations) for cystic fibrosis;Aslam AA;Cochrane Database Syst Rev,2017

4. Chinese experts consensus statement: diagnosis and treatment of cystic fibrosis (2023];Chinese Experts Cystic Fibrosis Consensus Committee; Chinese Alliance for Rare Lung Diseases; Chinese Alliance for Rare Diseases, Bronchiectasis‐China;Zhonghua Jie He He Hu Xi Za Zhi,2023

5. Systematic estimation of cystic fibrosis prevalence in Chinese and genetic spectrum comparison to Caucasians

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