×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.
23233322
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity.
23539503
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
A systematic approach to assessing the clinical significance of genetic variants.
24033266
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.
24367593
2013
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
21846512
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Sarcomeric hypertrophic cardiomyopathy: genetic profile in a Portuguese population.
22857948
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
CLINVAR
Sarcomeric hypertrophic cardiomyopathy: genetic profile in a Portuguese population.
22857948
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.
22517884
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Molecular effects of familial hypertrophic cardiomyopathy-related mutations in the TNT1 domain of cTnT.
22579624
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
22675533
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Correlation of molecular and functional effects of mutations in cardiac troponin T linked to familial hypertrophic cardiomyopathy: an integrative in silico/in vitro approach.
22334656
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Conduction abnormalities in pediatric patients with restrictive cardiomyopathy.
22260945
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
UNIPROT
Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
21846512
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.
22144547
2012
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
21551322
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
21310275
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
CLINVAR
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
21310275
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Myosin cross-bridges do not form precise rigor bonds in hypertrophic heart muscle carrying troponin T mutations.
21683708
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy.
20624503
2011
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy.
20978592
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
Biomarker
disease
GENOMICS_ENGLAND
The genetics of dilated cardiomyopathy.
20186049
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
GeneticVariation
disease
CLINVAR
Ubiquitin proteasome dysfunction in human hypertrophic and dilated cardiomyopathies.
20159828
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Cardiomyopathy-causing deletion K210 in cardiac troponin T alters phosphorylation propensity of sarcomeric proteins.
20079745
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
19324435
2010
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
0.900
CausalMutation
disease
CLINVAR
Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging.
20439259
2010