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Profile of tezacaftor/ivacaftor combination and its potential in the treatment of cystic fibrosis
Cystic fibrosis (CF) is a life-limiting autosomal recessive disease caused by dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) ion channel. Management of CF has traditionally relied upon managing complications of CFTR protein dysfunction and this has led to a steady impr...
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| Publicado no: | Ther Clin Risk Manag |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6710479/ https://ncbi.nlm.nih.gov/pubmed/31692517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TCRM.S165027 |
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