CFTR Modulators in People with Cystic Fibrosis: Real-World Evidence in France

Cystic fibrosis (CF) is a rare genetic multisystemic disease, the manifestations of which are due to mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein and can lead to respiratory insufficiency and premature death. CFTR modulators, which were developed in the pa...

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Detalles Bibliográficos
Autores principales: Regard, Lucile, Martin, Clémence, Burnet, Espérie, Da Silva, Jennifer, Burgel, Pierre-Régis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179538/
https://www.ncbi.nlm.nih.gov/pubmed/35681464
http://dx.doi.org/10.3390/cells11111769

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179538/
https://www.ncbi.nlm.nih.gov/pubmed/35681464
http://dx.doi.org/10.3390/cells11111769

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