rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
21846512
2012
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene.
19167105
2010
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
20160190
2010
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Sumoylation regulates lamin A function and is lost in lamin A mutants associated with familial cardiomyopathies.
18606848
2008
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.
16061563
2005
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy.
15140538
2004
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.
15372542
2004
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.
15219508
2004
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Mutations in LMNA were detected in four families (8%), three with familial (R89L , 959delT, R377H) and one with sporadic DCM (S573L ).
12628721
2003
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation.
14675861
2003
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.
12920062
2003
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes.
14684700
2003
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.
12486434
2002
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.
11897440
2002
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
11561226
2001
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy.
11792809
2001
rs59040894
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
0.700
GeneticVariation
UNIPROT
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
10580070
1999