Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist
@article{NarooieNejad2009GenotypingRO, title={Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist}, author={Mehrnaz Narooie-Nejad and Fereshteh Chitsazian and Betsabeh Khoramian Tusi and F. Mousavi and M. Houshmand and M. Rohani and Azam Hosseinipour and A. Rismanchian and E. Elahi}, journal={Molecular Vision}, year={2009}, volume={15}, pages={2155 - 2161} }
Purpose To assess whether loci other than GLC3A, GLC3B, and GLC3C are linked to primary congenital glaucoma (PCG). Methods The gene CYP1B1 at GLC3A was screened in 19 Iranian PCG probands who had been recruited mostly from among individuals of Turkish ethnicity and individuals from central and eastern Iran. The gene MYOC was screened in patients from this cohort who lacked CYP1B1 mutations and in ten patients previously shown not to carry CYP1B1 mutations. Family members of 19 probands without… CONTINUE READING
6 Citations
Glaucoma in Iran and Contributions of Studies in Iran to the Understanding of the Etiology of Glaucoma
- Medicine
- Journal of ophthalmic & vision research
- 2015
- 15
References
SHOWING 1-10 OF 29 REFERENCES
Molecular genetics of primary congenital glaucoma in Brazil.
- Medicine, Biology
- Investigative ophthalmology & visual science
- 2002
- 130
- PDF
Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma
- Biology, Medicine
- Journal of medical genetics
- 1999
- 153
- PDF
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
- Biology, Medicine
- The Journal of molecular diagnostics : JMD
- 2007
- 62
- PDF
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.
- Biology, Medicine
- Human molecular genetics
- 1997
- 581
- PDF
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus.
- Biology, Medicine
- Human molecular genetics
- 2000
- 215
- PDF
A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco
- Biology, Medicine
- Clinical genetics
- 2002
- 68
Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma.
- Biology, Medicine
- Investigative ophthalmology & visual science
- 2001
- 118
- PDF
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients.
- Biology, Medicine
- Molecular vision
- 2004
- 66
- PDF