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Congenital Aniridia: Clinic, Genetics, Therapeutics, and Prognosis
Congenital aniridia is a rare condition related to a deficiency in the PAX6 gene expression, which may occur as a result of a family inheritance or a sporadic occurrence. Additionally, this condition may occur as an isolated ocular phenotype or in association with a systemic syndrome. The most commo...
Autores principales: | Calvão-Pires, Pedro, Santos-Silva, R., Falcão-Reis, F., Rocha-Sousa, A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897488/ https://www.ncbi.nlm.nih.gov/pubmed/27355034 http://dx.doi.org/10.1155/2014/305350 |
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