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The combination of tezacaftor and ivacaftor in the treatment of patients with cystic fibrosis: clinical evidence and future prospects in cystic fibrosis therapy

Years of tremendous study have dawned a new era for the treatment of cystic fibrosis (CF). For years CF care was rooted in the management of organ dysfunction resulting from the mal-effects of absent anion transport through the CF transmembrane regulator (CFTR) protein. CFTR, an adenosine triphospha...

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Detalhes bibliográficos
Main Authors: Sherstin T. Lommatzsch, Jennifer L. Taylor-Cousar
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publishing 2019-04-01
Colecção:Therapeutic Advances in Respiratory Disease
Acesso em linha:https://doi.org/10.1177/1753466619844424
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