Rate of Lung Function Decline in People with Cystic Fibrosis Having a Residual Function Gene Mutation

INTRODUCTION: Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. Approximately 5% of people with CF have residual function (RF) CFTR mutations that result in partially retained CFTR activity. Published literature on d...

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Detalles Bibliográficos
Autores principales: Sawicki, Gregory S., Konstan, Michael W., McKone, Edward F., Moss, Richard B., Lubarsky, Barry, Suthoff, Ellison, Millar, Stefanie J., Pasta, David J., Mayer-Hamblett, Nicole, Goss, Christopher H., Morgan, Wayne J., Duncan, Margaret E., Yang, Yoojung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727051/
https://www.ncbi.nlm.nih.gov/pubmed/36319933
http://dx.doi.org/10.1007/s41030-022-00202-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727051/
https://www.ncbi.nlm.nih.gov/pubmed/36319933
http://dx.doi.org/10.1007/s41030-022-00202-y

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