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Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1. [electronic resource] by
- Stoilov, I
- Akarsu, A N
- Alozie, I
- Child, A
- Barsoum-Homsy, M
- Turacli, M E
- Or, M
- Lewis, R A
- Ozdemir, N
- Brice, G
- Aktan, S G
- Chevrette, L
- Coca-Prados, M
- Sarfarazi, M
Producer: 19980423
In:
American journal of human genetics vol. 62
Availability: No items available.
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