×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
An alternative splicing product of the lamin A/C gene lacks exon 10.
8621584
1996
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
10080180
1999
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
10580070
1999
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.
10662742
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.
10662742
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B).
10814726
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C gene.
10908904
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
10939567
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation.
11138304
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation.
11138304
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.
11503164
2001
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
11561226
2001
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
11561226
2001
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy.
11792809
2001
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy.
11792810
2001
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
We investigated the prevalence of lamin A/C (LMNA ) gene defects in familial and sporadic dilated cardiomyopathies (DCM) associated with atrioventricular block (AVB) or increased serum creatine-phosphokinase (sCPK), and the corresponding changes in myocardial and protein expression.
11897440
2002
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Identification of lamin A/C ( LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B.
12032588
2002
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
12714972
2003
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.
12920062
2003
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.
12920062
2003
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation.
14675861
2003
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes.
14684700
2003
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.
15372542
2004
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.
15972724
2005
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Gene symbol: LMNA. Disease: Cardiomyopathy, dilated, with conduction defect 1.
16156025
2005