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Multicenter Surveillance of Cystic Fibrosis in Korean Children
PURPOSE: Cystic fibrosis (CF), caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is rare among non-Caucasians. We aimed to identify the clinical features and CFTR mutations in Korean children. METHODS: We included 18 pediatric patients with CF diagnosed usin...
Autores principales: | Kim, Hyung Young, Hong, Soo-Jong, Ahn, Kangmo, Suh, Dong In, Noh, Shin Hye, Kim, Soo Yeon, Yu, Jinho, Ko, Jung Min, Lee, Min Goo, Kim, Kyung Won |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523417/ https://www.ncbi.nlm.nih.gov/pubmed/36174992 http://dx.doi.org/10.4168/aair.2022.14.5.494 |
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