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Primary Congenital Glaucoma and the Involvement of CYP1B1
Primary congenital glaucoma (PCG) is an autosomal recessive disorder in children due to the abnormal development of the trabecular meshwork and the anterior chamber angle. With an onset at birth to early infancy, PCG is highly prevalent in inbred populations and consanguinity is strongly associated...
Tallennettuna:
| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3085158/ https://ncbi.nlm.nih.gov/pubmed/21572728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0974-9233.75878 |
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