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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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Bibliografiske detaljer
Main Authors: Valdivieso, Angel Gabriel, Santa-Coloma, Tomás A.
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2013
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3757715/
https://ncbi.nlm.nih.gov/pubmed/24024153
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.redox.2012.11.007
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