×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Confirmation of cause and manner of death via a comprehensive cardiac autopsy including whole exome next-generation sequencing.
24298987
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Faster cross-bridge detachment and increased tension cost in human hypertrophic cardiomyopathy with the R403Q MYH7 mutation.
24928957
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
UNIPROT
Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered care.
25182012
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise.
24510615
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.
25524337
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy.
24888384
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic.
25558701
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophy.
23690394
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
A systematic approach to assessing the clinical significance of genetic variants.
24033266
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.
23299917
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Creatine kinase adenosine triphosphate and phosphocreatine energy supply in a single kindred of patients with hypertrophic cardiomyopathy.
23751935
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Detection of a large duplication mutation in the myosin-binding protein C3 gene in a case of hypertrophic cardiomyopathy.
23816408
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families.
23054336
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.
23782526
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human β-cardiac myosin motor function.
23798412
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells.
23290139
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Hypertrophic cardiomyopathy associated with left ventricular noncompaction cardiomyopathy and coronary fistulae: a case report. One genotype, three phenotypes?
24268868
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.
23782526
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy.
23711808
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
A systematic approach to assessing the clinical significance of genetic variants.
24033266
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
T1 measurements identify extracellular volume expansion in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy.
23549607
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophy.
23690394
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Cardiomyopathy mutations in the tail of β-cardiac myosin modify the coiled-coil structure and affect integration into thick filaments in muscle sarcomeres in adult cardiomyocytes.
24047955
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.
23283745
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.
24093860
2013