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

Ivaylo Stoilov(UConn Health), Nurten Akarsu(Hacettepe University), Ihuoma Alozie(UConn Health), Anne Child(St George's, University of London), Magda Barsoum‐Homsy(Université de Montréal), M. Erol Turaçlı(Ankara University), Meral Or(Gazi University), Richard A. Lewis(University of California, Davis), Nusret Özdemir(Cukurova University), Glen Brice(St George's, University of London), Sedat Aktan(Ankara University), Line Chevrette(Université de Montréal), Miguel Coca‐Prados(Yale University), Mansoor Sarfarazi(UConn Health)
The American Journal of Human Genetics
March 1, 1998
10.1086/301764
Cited by 392Open Access
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