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-Reference-Cited by-同舟云学术

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

Published:1998-03 Issue:3 Volume:62 Page:573-584
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Stoilov Ivaylo,Akarsu A. Nurten,Alozie Ihuoma,Child Anne,Barsoum-Homsy Magda,Turacli M. Erol,Or Meral,Lewis Richard A.,Ozdemir Nusret,Brice Glen,Aktan S. Gulderen,Chevrette Line,Coca-Prados Miguel,Sarfarazi Mansoor

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. A second locus (GLC3B) for primary congenital glaucoma (buphthalmos) maps to the 1p36 region;Akarsu;Hum Mol Genet,1996

2. A new concept of development of anterior chamber angle: its relationship to developmental glaucoma and other structural anomalies;Allen;Arch Ophthalmol,1955

3. The development of the trabecular meshwork and its abnormality in primary infantile glaucoma;Anderson;Trans Am Ophthalmol Soc,1981

4. Pathogenesis of congenital glaucoma;Barkan;Am J Ophthalmol,1955

5. Incidence and prognosis of childhood glaucoma;Barsoum-Homsy;Ophthalmology,1986

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