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>...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Book |
| Published: |
Journal of Clinical Research and Ophthalmology - Peertechz Publications,
2018-06-18.
|
| Subjects: | |
| Online Access: | Connect to this object online. |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|