Stoilov I.,1998
Stoilov I., Akarzu 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. 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. - Am.J.Hum.Genet., 1998, v. 62, p. 573-584.
