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Altered gene expression in slc4a11(−/−) mouse cornea highlights SLC4A11 roles
SLC4A11 is a H(+)/NH(3)/water transport protein, of corneal endothelial cells. SLC4A11 mutations cause congenital hereditary endothelial dystrophy and some cases of Fuchs endothelial corneal dystrophy. To probe SLC4A11’s roles, we compared gene expression in RNA from corneas of 17-week-old slc4a11(−...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536660/ https://www.ncbi.nlm.nih.gov/pubmed/34686736 http://dx.doi.org/10.1038/s41598-021-98921-w |