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A Single-Base Substitution in the Seed Region of miR-184 Causes EDICT Syndrome
PURPOSE. To investigate the cause of the syndrome characterized by endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (EDICT). METHODS. Previously a multigenerational family was reported that comprised 10 individuals affected by syndromal anterior segment dysgenesis. B...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Association for Research in Vision and Ophthalmology, Inc.
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3292370/ https://ncbi.nlm.nih.gov/pubmed/22131394 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.11-8783 |
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