Lumacaftor/ivacaftor combination for CF patients homozygous for Phe508del-CFTR

Cystic Fibrosis (CF) is a life-shortening inherited disease caused by the loss or dysfunction of the CF transmembrane conductance regulator (CFTR) channel activity resulting from mutations in the CFTR gene. Phe508del is the most prevalent mutation with approximately 90% of CF patients carries it on...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Drugs Today (Barc)
Autores principales: Zhang, Weiqiang, Zhang, Xiaoying, Zhang, Yanhui H., Stokes, Dennis C, Naren, Anjaparavanda P.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
Materias:
Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5495103/
https://ncbi.nlm.nih.gov/pubmed/27252987
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1358/dot.2016.52.4.2467205
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares