Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

GLAUCOMA 3, PRIMARY CONGENITAL, C

Known as: GLC3C 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Toward Primary Congenital Glaucoma GLC 3 B Gene Identification : The Case of Kazrin Gene
Primary Congenital Glaucoma (PCG) is an ocular disease that occurs before the age of 3 years, and results from malformation of… Expand
  • figure 1
  • table 1
Is this relevant?
2013
2013
LTBP2 gene analysis in the GLC3C-linked family and 94 CYP1B1-negative cases with primary congenital glaucoma
Purpose: Primary congenital glaucoma (isolated trabeculodysgensis, PCG) generally presents between birth and 3 years of age… Expand
Is this relevant?
2011
2011
Analysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucoma
PURPOSE Primary congenital glaucoma (PCG) is an autosomal recessive form of glaucoma that manifests within the first year of life… Expand
  • table 1
  • figure 1
  • table 2
  • figure 2
Is this relevant?
Review
2011
Review
2011
Primary Congenital Glaucoma and the Involvement of CYP1B1
Primary congenital glaucoma (PCG) is an autosomal recessive disorder in children due to the abnormal development of the… Expand
  • table 1
  • table 1
  • table 2
  • table 3
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Null mutations in LTBP2 cause primary congenital glaucoma.
Primary congenital glaucoma (PCG) is an autosomal-recessive condition characterized by high intraocular pressure (IOP), usually… Expand
Is this relevant?
2009
2009
Confirmation and further mapping of the GLC3C locus in primary congenital glaucoma.
We investigated the relationship between primary congenital glaucoma (PCG) in the Chinese Han population and its candidate locus… Expand
  • table 1
  • table 2
  • table 3
  • table 4
  • table 5
Is this relevant?
2009
2009
Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist
PURPOSE To assess whether loci other than GLC3A, GLC3B, and GLC3C are linked to primary congenital glaucoma (PCG). METHODS The… Expand
  • table 1
  • figure 1
  • figure 2
Is this relevant?
2003
2003
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients.
Primary congenital glaucoma (PCG) is an autosomal recessive disease, caused by unknown developmental defect(s) of the trabecular… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • table 3
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE