rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes.
|
22484823 |
2013 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes.
|
22484823 |
2013 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Exome analysis of two limb-girdle muscular dystrophy families: mutations identified and challenges encountered.
|
23155419 |
2012 |
rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Exome analysis of two limb-girdle muscular dystrophy families: mutations identified and challenges encountered.
|
23155419 |
2012 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics.
|
22275259 |
2012 |
rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.
|
22153487 |
2012 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.
|
22153487 |
2012 |
rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics.
|
22275259 |
2012 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Desmin myopathy.
|
14724127 |
2004 |
rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Desmin myopathy.
|
14724127 |
2004 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
|
10717012 |
2000 |
rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Desmin splice variants causing cardiac and skeletal myopathy.
|
11073539 |
2000 |
rs267607483
|
|
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Desmin splice variants causing cardiac and skeletal myopathy.
|
11073539 |
2000 |
rs267607483
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
|
10717012 |
2000 |