×
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
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
GeneticVariation
CLINVAR
A novel mutation in a large French-Canadian family with LGMD1B.
18714801 2008
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern.
20576434 2010
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
18035086 2007
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Mutations in LMNA modulate the lamin A--Nesprin-2 interaction and cause LINC complex alterations.
23977161 2013
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Novel c.367_369del LMNA mutation manifesting as severe arrhythmias, dilated cardiomyopathy, and myopathy.
22019351 2012
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Rare variant mutations identified in pediatric patients with dilated cardiomyopathy.
21483645 2011
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Sumoylation regulates lamin A function and is lost in lamin A mutants associated with familial cardiomyopathies.
18606848 2008
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
20160190 2010
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
16386954 2006
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy.
22177269 2012
×
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
GeneticVariation
CLINVAR
MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy.
21840938 2011
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy.
19875404 2009
×
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Abstracts from the 11th Annual Meeting of the ECCR (European Council for Cardiovascular Research), Nice, France, 29 September-1 October 2006.
16990647 2006
×
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
×
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
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
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
Cardioembolic stroke related to limb-girdle muscular dystrophy 1B.
23360689 2013
×
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
GeneticVariation
CLINVAR
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
18646565 2007
×
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
Primary prevention of sudden death in patients with lamin A/C gene mutations.
16407522 2006