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Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies
Two blinding corneal dystrophies, pediatric-onset congenital hereditary endothelial dystrophy (CHED) and some cases of late-onset Fuchs endothelial corneal dystrophy (FECD), are caused by SLC4A11 mutations. Three N-terminal SLC4A11 variants: v1, v2 and v3 are expressed in humans. We set out to deter...
Gardado en:
| Publicado en: | Sci Rep |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6609610/ https://ncbi.nlm.nih.gov/pubmed/31273259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-46094-y |
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