Molecular Genetic Study of Primary Congenital Glaucoma

Mansoor Sarfarazi, PhD
University of Connecticut Health Ce (Farmington, CT)
Year Awarded:
1993
Grant Duration:
April 1, 1993 to March 31, 1994
Disease:
Glaucoma
Award Amount:
$49,902
Grant Reference ID:
G1993322
Award Type:
Standard
Award Region:
US Northeastern

Molecular Genetic Study of Primary Congenital Glaucoma

Details


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.  

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