×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy.
22177269
2012
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
CausalMutation
CLINVAR
Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene.
19167105
2010
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies.
24375749
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
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, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation.
21085127
2011
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
CausalMutation
CLINVAR
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
27760138
2016
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Systematic identification of pathological lamin A interactors.
24623722
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
18585512
2008
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
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, Familial Idiopathic
1.000
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, Familial Idiopathic
1.000
CausalMutation
CLINVAR
Cardiac arrest and left ventricular fibrosis in a Finnish family with the lamin A/C mutation.
18031519
2008
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
23183350
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Laminopathies in Russian families.
18564364
2008
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
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, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Our in vivo and in vitro results question the relationship of causality between LMNA mutations and the development of heart failure in some DCM patients and therefore, the reliability of genetic counselling.
16061563
2005
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
24503780
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Familial Idiopathic
1.000
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, Familial Idiopathic
1.000
GeneticVariation
CLINVAR
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.
15372542
2004