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Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family
AIMS—To establish a clinical and molecular diagnosis in a family with late onset lattice corneal dystrophy. METHODS—Linkage analysis, single strand conformation polymorphism (SSCP) analysis, and direct sequencing of genomic DNA were performed. A review of the patients' clinical symptoms and sig...
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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2000
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1723421/ https://ncbi.nlm.nih.gov/pubmed/10729296 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.84.4.390 |
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