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Loss of ion transporters and increased unfolded protein response in Fuchs’ dystrophy
PURPOSE: Fuchs’ endothelial corneal dystrophy (FECD), which affects approximately 5% of the population over 40 in the U.S.A., is a major cause of corneal transplantation. FECD is associated with mutations of a variety of unrelated genes: SLC4A11, COL8A2, TCF8, and LOXHD1. The current pathological de...
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| Publicado no: | Mol Vis |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Molecular Vision
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4265779/ https://ncbi.nlm.nih.gov/pubmed/25548511 |
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