Molecular Genetic Study of Primary Congenital Glaucoma

Publications

Stoilov, I., et al. (1997) 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. Hum. Mol. Genet. 2:21.  

Akarsu, A.N., Turacli, M.E., Aktan, S.G., Hossain, A., et al. (1996) Exclusion of primary congenital glaucoma (Buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11. Am. J. Med. Genet. 61:290-292.  

Akarsu, A.N., Turacli, M.E., Aktan, S.G., Barsoum-Homsy, M., et al. (1996) A second locus (GLC3B) for Primary Congenital Glaucoma (Buphthalmos) maps to the 1p36 region. Hum. Mol. Genet. 5(8):1199-1203.  

Sarfarazi, M., Akarsu, A.N., Hossain, A., Turacli, M.E., et al. (1995) Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics. 30:171-177.