Mitochondrial alterations and oxidative stress in cystic fibrosis
Abstract: Cystic fibrosis (CF) is the most frequent autosomal recessive disease and is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Since the discovery of the deletion in the phenylalanine 508 site (ΔF508) of the CFTR gene, the study of its function...
Guardado en:
| Autor principal: | Valdivieso, Ángel Gabriel |
|---|---|
| Formato: | Parte de libro |
| Lenguaje: | Inglés |
| Publicado: |
Springer Nature
2022
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| Materias: | |
| Acceso en línea: | https://repositorio.uca.edu.ar/handle/123456789/14243 |
| Aporte de: |
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