FAQ

GLAUCOMA 3, PRIMARY CONGENITAL, C

Known as: GLC3C 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2009-2013
01220092013

Papers overview

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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… (More)
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2011
2011
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… (More)
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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… (More)
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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… (More)
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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… (More)
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