Molecular basis of oculocutaneous albinism type 1 in Lebanese patients
Oculocutaneous albinism type 1 (OCA1) results from mutations in the tyrosinase gene, which lead to partial or complete loss of activity of the corresponding enzyme. A large number of mutations have been identified worldwide, providing insight into the pathogenesis of the disorder. We performed ophth...
Saved in:
| Main Author: | |
|---|---|
| Other Authors: | , , , , , |
| Format: | article |
| Published: |
2005
|
| Online Access: | http://hdl.handle.net/10725/11095 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php https://link.springer.com/article/10.1007/s10038-005-0257-5 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|