×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
Biomarker
disease
CLINGEN
New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy.
30517146
2018
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration.
28132693
2017
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
Biomarker
disease
GENOMICS_ENGLAND
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita.
27933661
2017
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita.
27933661
2017
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
One in seven colorectal cancer patients is under 50, US study shows.
26809612
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
Biomarker
disease
CLINGEN
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients.
27105866
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
New massive parallel sequencing approach improves the genetic characterization of congenital myopathies.
26841830
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients.
27105866
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disorders.
27357428
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients.
27105866
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing.
26809617
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
New massive parallel sequencing approach improves the genetic characterization of congenital myopathies.
26841830
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
A recurrent copy number variation of the NEB triplicate region: only revealed by the targeted nemaline myopathy CGH array.
26197980
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.
27854218
2016
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
Biomarker
disease
CLINGEN
Effect of levosimendan on the contractility of muscle fibers from nemaline myopathy patients with mutations in the nebulin gene.
25949787
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth.
26578207
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
"Bilateral foot-drop as predominant symptom in nebulin (NEB) gene related ""core-rod"" congenital myopathy."
26403434
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
25356970
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
Biomarker
disease
CLINGEN
Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy.
26123491
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
Potential toxicity of pesticides in freshwater environments: passive sampling, exposure and impacts on biofilms: the PoToMAC project.
25205148
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
CausalMutation
disease
CLINVAR
Nemaline myopathy type 2 (NEM2): two novel mutations in the nebulin (NEB) gene.
24056153
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth.
26578207
2015
×
Entrez Id:
4703
Gene Symbol:
NEB
NEB
0.920
GeneticVariation
disease
CLINVAR
"Bilateral foot-drop as predominant symptom in nebulin (NEB) gene related ""core-rod"" congenital myopathy."
26403434
2015