Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,258,701 papers from all fields of science
Search
Sign In
Create Free Account
GLAUCOMA 3, PRIMARY INFANTILE, B
Known as:
Glaucoma, primary congenital, type 3B
, GLC3, TYPE B
, Glaucoma, Primary Congenital, Type B
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
GLC3B gene
Broader (1)
Glaucoma
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
Soumaya El Akil
,
A. Belmouden
2019
Corpus ID: 76649518
Primary Congenital Glaucoma (PCG) is an ocular disease that occurs before the age of 3 years, and results from malformation of…
Expand
2011
2011
Analysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucoma
J. Lee
,
C. Ki
,
+4 authors
C. Kee
Molecular Vision
2011
Corpus ID: 17517202
Purpose Primary congenital glaucoma (PCG) is an autosomal recessive form of glaucoma that manifests within the first year of life…
Expand
2009
2009
Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist
M. Narooie-Nejad
,
F. Chitsazian
,
+6 authors
E. Elahi
Molecular Vision
2009
Corpus ID: 9009375
Purpose To assess whether loci other than GLC3A, GLC3B, and GLC3C are linked to primary congenital glaucoma (PCG). Methods The…
Expand
Highly Cited
2003
Highly Cited
2003
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients
R. Sitorus
,
S. Ardjo
,
B. Lorenz
,
M. Preising
Journal of Medical Genetics
2003
Corpus ID: 29671974
Primary congenital glaucoma (PCG) is an autosomal recessive disease, caused by unknown developmental defect(s) of the trabecular…
Expand
Review
2000
Review
2000
[Genetic studies on primary open angle glaucoma].
J. Szaflik
,
A. Ambroziak
,
J. Bal
,
M. Gacek
Klinika oczna
2000
Corpus ID: 2761866
Case work presents the newest studies on molecular genetics in primary open angle glaucoma. The molecular genetics in all types…
Expand
2000
2000
Altered protein mannosylation in developing cerebral cortex by streptomycin
Mario D. Alperin
,
J. Calandria
,
H. Carminatti
,
Victor P. Idoyaga-Vargas
NeuroReport
2000
Corpus ID: 32680511
Our research objective was to characterize the biochemical effect of streptomycin during postnatal rat cerebral cortex…
Expand
1984
1984
Glycosylation and processing of high-mannose oligosaccharides of thyroid-stimulating hormone subunits: comparison to nonsecretory cell glycoproteins.
C. Ronin
,
B. Stannard
,
I. Rosenbloom
,
J. Magner
,
B. Weintraub
Biochemistry
1984
Corpus ID: 21805962
Thyroid-stimulating hormone (TSH) subunit glycosylation was compared to that of total cell glycoproteins in mouse thyrotropic…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE