Llwytho...
Myocilin Mutations Are Not a Major Cause of Primary Congenital Glaucoma in Iranian Patients
PURPOSE: To assess the frequency of mutations in the Myocilin (MYOC) gene in Iranian patients affected with primary congenital glaucoma (PCG). METHODS: The individuals evaluated herein are among a larger cohort of 100 patients who had previously been screened for CYP1B1 mutations. Eighty subjects ca...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Ophthalmic Research Center
2010
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3380681/ https://ncbi.nlm.nih.gov/pubmed/22737338 |
| Tagiau: |
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