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Classic Lattice Corneal Dystrophy Associated with Monoclonal Gammopathy Following Exclusion of a TGFBI Mutation
PURPOSE: To report the association of phenotypic features characteristic of lattice corneal dystrophy with a monoclonal gammopathy of undetermined significance following exclusion of a coding region mutation in TGFBI. DESIGN: Case report METHODS: Slit lamp examination was performed, as well as colle...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2009
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2784604/ https://ncbi.nlm.nih.gov/pubmed/19092416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/ICO.0b013e31818200f4 |
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