A Laboratory Study on the Molecular Basis of Primary Congenital Glaucoma
<p><strong>Purpose:</strong> To detect pathogenic mutations in cytochrome P450 family1 subfamily B polypeptide1</p><p>(CYP1B1) gene in nineteen sporadic Primary congenital glaucoma (PCG) cases and to identify patients</p><p>lacking CYP1B1 mutations.</p>...
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| Main Authors: | , , |
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| Format: | Book |
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Journal of Clinical Research and Ophthalmology - Peertechz Publications,
2018-06-18.
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| Online Access: | Connect to this object online. |
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