×
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
CausalMutation
CLINVAR
Genetic Testing in Pediatric Left Ventricular Noncompaction.
29212898
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Dilated
0.490
CausalMutation
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
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
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
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
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
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
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
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
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
CausalMutation
CLINVAR
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
24503780
2014
×
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
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
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
CausalMutation
CLINVAR
Myosinopathies: pathology and mechanisms.
22918376
2013
×
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
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
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
Genetic testing for dilated cardiomyopathy in clinical practice.
22464770
2012
×
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
CausalMutation
CLINVAR
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.
22949430
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
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
21750094
2011