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...

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Detalles Bibliográficos
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
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
Materias:
Original Article
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

Internet

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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