×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands.
19477645
2009
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands.
19477645
2009
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs.
23153285
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.
24691700
2015
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
A rare mutation in MYH7 gene occurs with overlapping phenotype.
25576864
2015
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy.
18660445
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
16983074
2006
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
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, Dilated
0.490
GeneticVariation
CLINVAR
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
19412328
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
19412328
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Effects of pathogenic proline mutations on myosin assembly.
22155079
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Electrocardiographic features of sarcomere mutation carriers with and without clinically overt hypertrophic cardiomyopathy.
21943931
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy.
23313350
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.
22337857
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience.
23349452
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Genetic testing for dilated cardiomyopathy in clinical practice.
22464770
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Genetic testing for dilated cardiomyopathy in clinical practice.
22464770
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Genetic Testing in Pediatric Left Ventricular Noncompaction.
29212898
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Haplotype sharing test maps genes for familial cardiomyopathies.
20573160
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Human growth hormone stimulates somatomedin C/insulin-like growth factor I production by the human lymphoid cell line, IM-9.
2753225
1989
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.
17351073
2007
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction.
26025024
2015
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
15769782
2005
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes.
19854198
2010
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
11106718
2000