|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.
|
23396983 |
2013 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.
|
28408708 |
2017 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy.
|
8989109 |
1996 |
|
| 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 |
GeneticVariation
|
disease |
CLINVAR |
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.
|
12860912 |
2003 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
|
12707239 |
2003 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Sudden death due to troponin T mutations.
|
9060892 |
1997 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy.
|
9140840 |
1997 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy.
|
9140840 |
1997 |
|
| 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 |
GeneticVariation
|
disease |
UNIPROT |
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
|
8205619 |
1994 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy.
|
26914223 |
2016 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
|
12707239 |
2003 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy.
|
11034944 |
2000 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy.
|
7898523 |
1995 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience.
|
23349452 |
2013 |
|
| 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 |
GeneticVariation
|
disease |
UNIPROT |
A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy.
|
9482583 |
1998 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
|
| 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 |
GeneticVariation
|
disease |
UNIPROT |
Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy.
|
12974739 |
2003 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy.
|
10525521 |
1999 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
|
20031601 |
2009 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
UNIPROT |
Mutations profile in Chinese patients with hypertrophic cardiomyopathy.
|
15563892 |
2005 |
|
| Entrez Id: |
7139 |
| Gene Symbol: |
TNNT2 |
TNNT2
|
0.900 |
GeneticVariation
|
disease |
CLINVAR |
Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging.
|
20439259 |
2010 |