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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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| Veröffentlicht in: | Int Sch Res Notices |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Hindawi Publishing Corporation
2014
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| Schlagworte: | |
| Online Zugang: | 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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