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Mutations associated with Dent's disease affect gating and voltage dependence of the human anion/proton exchanger ClC-5
Dent's disease is associated with impaired renal endocytosis and endosomal acidification. It is linked to mutations in the membrane chloride/proton exchanger ClC-5; however, a direct link between localization in the protein and functional phenotype of the mutants has not been established until...
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| Publicado no: | Front Physiol |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4436585/ https://ncbi.nlm.nih.gov/pubmed/26042048 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2015.00159 |
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