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Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India
BACKGROUND: Mutations in COL8A2 gene which encodes the collagen alpha-2 (VIII) chain have been identified in both familial and sporadic cases of Fuchs endothelial corneal dystrophy (FECD). Heterozygous mutations in the SLC4A11 gene are also known to cause late-onset FECD. Therefore we screened for C...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2834660/ https://ncbi.nlm.nih.gov/pubmed/20144242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2415-10-3 |
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