CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States

Author:

Lim Sing-Hui,Tran-Viet Khanh-Nhat,Yanovitch Tammy L.,Freedman Sharon F.,Klemm Thomas,Call Whitney,Powell Caldwell,Ravichandran Ajay,Metlapally Ravikanth,Nading Erica B.,Rozen Steve,Young Terri L.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference44 articles.

1. Shields’ Textbook of Glaucoma;Allingham,2005

2. Abu-Amero KK, Edward DP. Primary congenital glaucoma. In: Pagon RA, ed.-in-chief; Bird TD, Dolan CR, Stephens K, Adam MP, eds. GeneReviews. Seattle: University of Washington; September 30, 2004; last revision August 25, 2011. Available at: www.ncbi.nih.gov/books/NBK1135. Accessed February 10, 2012.

3. Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma;Dimasi;Clin Genet,2007

4. Childhood blindness in the context of VISION 2020—the right to sight;Gilbert;Bull World Health Org,2001

5. Primary congenital glaucoma and the involvement of CYP1B1;Kaur;Middle East Afr J Ophthalmol,2011

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