REFERENCES
- Henson D B, Thampy R. Preventing blindness from glaucoma. Br Med J 2005; 331: 120–121
- Plasilova M, Stoilov I, Sarfarazi M, Kadasi L, Ferakova E, Ferak V. Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. J Med Genet 1999; 36: 290–294
- Dandona L, Williams J D, Williams B C, Rao G N. Population-based assessment of childhood blindness in southern India. Arch Ophthalmol. 1998; 116: 545–546
- Sarfarazi M, Akarsu A N, Hossain A, Turacli M E, Aktan S G, Barsoum-Homsy M, Chevrette L, Sayli B S. Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 1995; 30: 171–177
- Akarsu A N, Turacli M E, Aktan S G, Barsoum-Homsy M, Chevrette L, Sayli B S, Sarfarazi M. A second locus (GLC3B) for primary congenital glaucoma (buphthalmos) maps to the 1p36 region. Hum Mol Genet 1996; 5: 1199–1203
- Stoilov I R, Sarfarazi M. The third genetic locus (GLC3C) for primary congenital glaucoma (PCG) maps to chromosome 14q24.3. Invest Ophthalmol Visual Sci. 2002; 43, E-Abstract 3015
- Stoilov I, Akarsu A N, Sarfarazi M. Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet 1997; 6: 641–647
- Sarfarazi M, Stoilov I, Schenkman J B. Genetics and biochemistry of primary congenital glaucoma. Ophthalmol Clin N Am 2003; 16: 543–554
- Wolff R, Gemmil R. Purifying and analysing genomic DNA. Genome analysis. A laboratory manual, B Bruce, E D Green, S Klapholz, R M Myeres, J Roskans. CSHL Press. 1998
- Stoilov I, Akarsu 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; 62: 573–584
- Stoilov I R, Costa V P, Vasconcellos J P, Melo M B, Betinjane A J, Carani J C, Oltrogge E V, Sarfarazi M. Molecular genetics of primary congenital glaucoma in Brazil. Invest Ophthalmol Visual Sci. 2002; 43: 1820–1827
- Mashima Y, Suzuki Y, Sergeev Y, Ohtake Y, Tanino T, Kimura I, Miyata H, Aihara M, Tanihara H, Inatani M, Azuma N, Iwata T, Araie M. Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma. Invest Ophthalmol Visual Sci 2001; 42: 2211–2216
- Reddy A B, Kaur K, Mandal A K, Panicker S G, Thomas R, Hasnain S E, Balasubramanian D, Chakrabarti S. Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Mol Vision. 2004; 30: 696–702
- Panicker S G, Reddy A B, Mandal A K, Ahmed N, Nagarajaram H A, Hasnain S E, Balasubramanian D. Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. Invest Ophthalmol Vis Sci. 2002; 43: 1358–1366
- Murray J, Cuckle H, Taylor G, Littlewood J, Hewison J. Screening for cystic fibrosis. Health Technol Assess. 1998; 3(8)31–81
- Kumaramanickavel G, Joseph B, Vidhya A, Arokiasamy T, Shridhara Shetty N. Consanguinity and ocular genetic diseases in South India: analysis of a five-year study. Community Genet 2002; 5(3)182–185