×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
21750094
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy.
21211974
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
24119082
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.
25448463
2014
×
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
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
GeneticVariation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
15556047
2004
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Prognostic Relevance of Gene-Environment Interactions in Patients With Dilated Cardiomyopathy: Applying the MOGE(S) Classification.
26383716
2015
×
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
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
The sarcomeric M-region: a molecular command center for diverse cellular processes.
25961035
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
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.
24664454
2014
×
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
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
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
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
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
GeneticVariation
CLINVAR
Genetic testing for dilated cardiomyopathy in clinical practice.
22464770
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
GeneticVariation
CLINVAR
Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families.
23054336
2013
×
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
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
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
20031619
2009
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
CLINVAR
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.
24664454
2014