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SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy
Congenital hereditary endothelial dystrophy (CHED) is a rare autosomal recessive disorder of the corneal endothelium characterized by nonprogressive bilateral corneal edema and opacification present at birth. Here we review the current knowledge on the role of the SLC4A11 gene, protein, and its muta...
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| Publicado no: | Biomed Res Int |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4588344/ https://ncbi.nlm.nih.gov/pubmed/26451371 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/475392 |
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