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A Novel Decorin Gene Mutation in Congenital Hereditary Stromal Dystrophy: A Korean Family
A 43-year-old man developed decreased vision in the right eye that had persisted for seven years. Under slit lamp examination, corneal clouding was noted with normal endothelium and ocular structure. From the clinical evidence, we suspected that the patient had congenital hereditary stromal dystroph...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The Korean Ophthalmological Society
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3408537/ https://ncbi.nlm.nih.gov/pubmed/22870031 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3341/kjo.2012.26.4.301 |
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