The American Journal of Human Genetics
Volume 62, Issue 3, March 1998, Pages 573-584
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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Primary congenital glaucoma
CYP1B1
Homology modeling
Chromosome 2p21
Glaucoma, primary congenital
Cytochrome P4501B1
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Copyright © 1998 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.