×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Cellular processing of myocilin.
24732711
2014
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Compound heterozygote myocilin mutations in a pedigree with high prevalence of primary open-angle glaucoma.
23304066
2012
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Low prevalence of myocilin mutations in an African American population with primary open-angle glaucoma.
22933836
2012
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Variable clinical spectrum of the myocilin Gln368X mutation in a Dutch family with primary open angle glaucoma.
20021252
2010
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Heterozygous expression of myocilin glaucoma mutants increases secretion of the mutant forms and reduces extracellular processed myocilin.
19023451
2008
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Role of MYOC and OPTN sequence variations in Spanish patients with primary open-angle glaucoma.
17615537
2007
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Myocilin variants in Indian patients with open-angle glaucoma.
17562996
2007
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Myocilin analysis by DHPLC in French POAG patients: increased prevalence of Q368X mutation.
12872267
2003
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Rapid mutation detection by the transgenomic wave analyser DHPLC identifies MYOC mutations in patients with ocular hypertension and/or open angle glaucoma.
11815346
2002
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Founder TIGR/myocilin mutations for glaucoma in the Québec population.
12189160
2002
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier.
11535458
2001
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
MYOC mutation frequency in primary open-angle glaucoma patients from Western Switzerland.
11803488
2001
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucoma.
10815160
2000
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
A novel mutation in the GLC1A gene causes juvenile open-angle glaucoma in 4 families from the Italian region of Puglia.
9639450
1998
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
GeneticVariation
disease
CLINVAR
Identification of a gene that causes primary open angle glaucoma.
9005853
1997
×
Entrez Id:
110806290
Gene Symbol:
MYOCOS
MYOCOS
0.100
CausalMutation
disease
CLINVAR