CFTR activity and mitochondrial function()

Cystic Fibrosis (CF) is a frequent and lethal autosomal recessive disease, caused by mutations in the gene encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). Before the discovery of the CFTR gene, several hypotheses attempted to explain the etiology of this disease, including t...

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Detalles Bibliográficos
Autores principales: Valdivieso, Angel Gabriel, Santa-Coloma, Tomás A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757715/
https://www.ncbi.nlm.nih.gov/pubmed/24024153
http://dx.doi.org/10.1016/j.redox.2012.11.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757715/
https://www.ncbi.nlm.nih.gov/pubmed/24024153
http://dx.doi.org/10.1016/j.redox.2012.11.007

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