×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Connexin 43 remodeling induced by LMNA gene mutation Glu82Lys in familial dilated cardiomyopathy with atrial ventricular block.
20497714
2010
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
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
0.100
CausalMutation
disease
CLINVAR
A conserved splicing mechanism of the LMNA gene controls premature aging.
21875900
2011
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Long-term outcome and risk stratification in dilated cardiolaminopathies.
18926329
2008
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
A laminopathic mutation disrupting lamin filament assembly causes disease-like phenotypes in Caenorhabditis elegans.
21653823
2011
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.
15219508
2004
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
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
0.100
CausalMutation
disease
CLINVAR
Genetic basis of familial dilated cardiomyopathy patients undergoing heart transplantation.
26899768
2016
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
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
0.100
CausalMutation
disease
CLINVAR
Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype.
20155465
2010
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA.
27876398
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
17347251
2007
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardiomyopathy and ventricular tachycardia.
17987279
2008
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Progerin expression disrupts critical adult stem cell functions involved in tissue repair.
25567453
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation.
19842191
2009
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Homozygous lamin A/C familial lipodystrophy R482Q mutation in autosomal recessive Emery Dreifuss muscular dystrophy.
23313286
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.
11897440
2002
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
26098624
2015
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture.
23969228
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
28679633
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Bayesian latent class models with conditionally dependent diagnostic tests: a case study.
18551515
2008
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
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
0.100
CausalMutation
disease
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
0.100
CausalMutation
disease
CLINVAR
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.
12628721
2003
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
0.100
CausalMutation
disease
CLINVAR
Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling.
23427149
2013