×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
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
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain.
25935763
2015
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.
25524337
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
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
Restrictive cardiomyopathy
0.110
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
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Conduction abnormalities in pediatric patients with restrictive cardiomyopathy.
22260945
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
GeneticVariation
CLINVAR
Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathy.
20818890
2010
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
A fetus with hypertrophic cardiomyopathy, restrictive, and single-ventricle physiology, and a beta-myosin heavy chain mutation.
20394946
2010
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathy.
20800588
2010
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
GeneticVariation
BEFREE
Here we report the first pediatric case of restrictive cardiomyopathy secondary to a de novo mutation in the cardiac myosin heavy chain gene MYH7 .
18380764
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.
18076673
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
GeneticVariation
LHGDN
Here we report the first pediatric case of restrictive cardiomyopathy secondary to a de novo mutation in the cardiac myosin heavy chain gene MYH7 .
18380764
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Here we report the first pediatric case of restrictive cardiomyopathy secondary to a de novo mutation in the cardiac myosin heavy chain gene MYH7 .
18380764
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].
17125710
2006
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Restrictive cardiomyopathy
0.110
CausalMutation
CLINVAR
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
12707239
2003