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Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies
SLC4A11, a member of the SLC4 family of bicarbonate transporters, is a widely expressed integral membrane protein, abundant in kidney and cornea. Mutations of SLC4A11 cause some cases of the blinding corneal dystrophies, congenital hereditary endothelial dystrophy, and Fuchs endothelial corneal dyst...
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| Publicado no: | Am J Physiol Cell Physiol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Physiological Society
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5130586/ https://ncbi.nlm.nih.gov/pubmed/27558157 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00078.2016 |
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