Molecular characterization of CYP1B1 in primary congenital glaucoma in Pakistan
Primary congenital glaucoma (PCG) is the foremost cause of blindness in children. In PCG the optic nerve damage and permanent loss of vision occurs because of developmental defects of trabecular meshwork of the eye. The mode of inheritance of PCG is mostly autosomal recessive, so, its incidence is...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
2017
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| Subjects: | |
| Online Access: | http://eprints.unisza.edu.my/5978/1/FH02-FP-18-13168.pdf http://eprints.unisza.edu.my/5978/ |
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