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. (Q24538817)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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. |
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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. (English)
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I Stoilov
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A N Akarsu
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I Alozie
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A Child
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M Barsoum-Homsy
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M E Turacli
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M Or
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R A Lewis
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N Ozdemir
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G Brice
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S G Aktan
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L Chevrette
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M Coca-Prados
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M Sarfarazi
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