×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope.
29943882
2018
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Next-Generation Sequencing to Diagnose Muscular Dystrophy, Rhabdomyolysis, and HyperCKemia.
29382405
2018
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
28679633
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
28679633
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Limb-girdle muscular dystrophy with severe heart failure overlapping with lipodystrophy in a patient with LMNA mutation p.Ser334del.
27585670
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Lamin A/C -Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation.
28790152
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.
29237675
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.
29149195
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Massive parallel sequencing questions the pathogenic role of missense variants in dilated cardiomyopathy.
27886618
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.
28798025
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly.
27723096
2017
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers.
27884249
2016
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Prognostic Relevance of Gene-Environment Interactions in Patients With Dilated Cardiomyopathy: Applying the MOGE(S) Classification.
26383716
2015
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159
2015
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
GeneticVariation
CLINVAR
Evaluation of damaging effects of splicing mutations: validation of an in vitro method for diagnostic laboratories.
24915601
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
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, Dilated
0.500
CausalMutation
CLINVAR
Lamin A/C mutations in dilated cardiomyopathy.
24846508
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
CausalMutation
CLINVAR
Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects.
24058181
2014
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
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, Dilated
0.500
CausalMutation
CLINVAR
Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.
23853504
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Cardiomyopathy, Dilated
0.500
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, Dilated
0.500
GeneticVariation
CLINVAR
Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling.
23427149
2013
×
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
CausalMutation
CLINVAR
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
23183350
2013