लोड हो रहा है...
Compound heterozygous mutations in CYP1B1 gene leads to severe primary congenital glaucoma phenotype
AIM: To identify the novel mutation alleles in the CYP1B1 gene of primary congenital glaucoma (PCG) patients at Shandong Province of China, and investigate their correlation with glaucomatous features. METHODS: The DNA from the peripheral blood of 13 congenital glaucoma patients and 50 ethnically ma...
में बचाया:
| में प्रकाशित: | Int J Ophthalmol |
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| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
International Journal of Ophthalmology Press
2019
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6580207/ https://ncbi.nlm.nih.gov/pubmed/31236345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2019.06.05 |
| टैग : |
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