Corpus ID: 9009375

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}
}
  • Mehrnaz Narooie-Nejad, Fereshteh Chitsazian, +6 authors E. Elahi
  • Published 2009
  • Medicine, Biology
  • Molecular Vision
  • 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
    Genetic Heterogeneity in Moroccan Primary Congenital Glaucoma Patients
    • 1
    • Highly Influenced
    • PDF
    Glaucoma in Iran and Contributions of Studies in Iran to the Understanding of the Etiology of Glaucoma
    • 15
    Pediatric genetic diseases causing glaucoma.
    • 3
    Pediatric glaucoma: current perspectives
    • 3
    • PDF
    Gene-Finding Strategy in Glaucoma

    References

    SHOWING 1-10 OF 29 REFERENCES
    Molecular genetics of primary congenital glaucoma in Brazil.
    • 130
    • PDF
    CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
    • 62
    • PDF
    A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco
    • 68
    Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma.
    • 118
    • PDF
    Myocilin gene implicated in primary congenital glaucoma
    • 87
    Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients.
    • 66
    • PDF
    Contributions of MYOC and CYP1B1 mutations to JOAG
    • 46
    • PDF