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Genome-wide Linkage Scan in Fuchs Endothelial Corneal Dystrophy
PURPOSE: To perform a genome-wide linkage screen with a single-nucleotide polymorphism (SNP) linkage panel to identify regions of genetic linkage in Fuchs endothelial corneal dystrophy (FECD) and to analyze affected individuals for mutations in the COL8A2 gene. METHODS: Ninety-two individuals from 2...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2712757/ https://ncbi.nlm.nih.gov/pubmed/18502986 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.08-1839 |
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