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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...

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Dades bibliogràfiques
Publicat a:Int Sch Res Notices
Autors principals: Calvão-Pires, Pedro, Santos-Silva, R., Falcão-Reis, F., Rocha-Sousa, A.
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2014
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4897488/
https://ncbi.nlm.nih.gov/pubmed/27355034
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/305350
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