Chloride conductance and genetic background modulate the cystic fibrosis phenotype of ΔF508 homozygous twins and siblings
To investigate the impact of chloride (Cl(–)) permeability, mediated by residual activity of the cystic fibrosis transmembrane conductance regulator (CFTR) or by other Cl(–) channels, on the manifestations of cystic fibrosis (CF), we determined Cl(–) transport properties of the respiratory and intes...
Збережено в:
| Опубліковано в:: | J Clin Invest |
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| Автори: | , , , , , , , , , , , |
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
American Society for Clinical Investigation
2001
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| Предмети: | |
| Онлайн доступ: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC200980/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11733566/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI12108 |
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