|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Study familial hypertrophic cardiomyopathy using patient-specific induced pluripotent stem cells.
|
25209314 |
2014 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
A novel de novo mutation of β-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy.
|
25189259 |
2014 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
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
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human β-cardiac myosin motor function.
|
23798412 |
2013 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
|
15856146 |
2005 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
A mouse model of familial hypertrophic cardiomyopathy.
|
8614836 |
1996 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
|
1552912 |
1992 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Expression of a missense mutation in the messenger RNA for beta-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy.
|
1634614 |
1992 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
|
1430197 |
1992 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.
|
1944483 |
1991 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene.
|
2144212 |
1990 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
Hypertrophic Cardiomyopathy
|
0.800 |
Biomarker |
CLINGEN |
A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.
|
1975517 |
1990 |