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
Open Access
- 1 March 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (3) , 573-584
- https://doi.org/10.1086/301764
Abstract
No abstract availableKeywords
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