|
Hereditary Motor and Sensory-Neuropathy Type II
|
|
0.700 |
CausalMutation
|
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
|
Hereditary Motor and Sensory-Neuropathy Type II
|
|
0.700 |
CausalMutation
|
CLINVAR |
Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.
|
23582089 |
2013 |
|
Hereditary Motor and Sensory-Neuropathy Type II
|
|
0.700 |
CausalMutation
|
CLINVAR |
Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy.
|
22177269 |
2012 |
|
Cardiomyopathy, Dilated
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy.
|
22177269 |
2012 |
|
Hereditary Motor and Sensory-Neuropathy Type II
|
|
0.700 |
CausalMutation
|
CLINVAR |
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
|
20160190 |
2010 |
|
Cardiomyopathy, Dilated
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
|
20160190 |
2010 |
|
Cardiomyopathy, Dilated
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
|
18585512 |
2008 |
|
Hereditary Motor and Sensory-Neuropathy Type II
|
|
0.700 |
CausalMutation
|
CLINVAR |
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
|
18646565 |
2007 |
|
Cardiomyopathy, Dilated
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
|
18646565 |
2007 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
|
24503780 |
2014 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
Systematic identification of pathological lamin A interactors.
|
24623722 |
2014 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
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 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
|
23183350 |
2013 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
|
21846512 |
2012 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
BEFREE |
The presumed pathogenic mutations were distributed with one case of suspected HCM and DCM (MYH7; p.R442H), one case of suspected DCM (LMNA; p.R471H), and two cases of suspected ARVC (PKP2; p.R79X and LMNA; p.R644C).
|
22177269 |
2012 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
The presumed pathogenic mutations were distributed with one case of suspected HCM and DCM (MYH7; p.R442H), one case of suspected DCM (LMNA; p.R471H), and two cases of suspected ARVC (PKP2; p.R79X and LMNA; p.R644C).
|
22177269 |
2012 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
|
20160190 |
2010 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
|
20160190 |
2010 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene.
|
19167105 |
2010 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
|
18585512 |
2008 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Sumoylation regulates lamin A function and is lost in lamin A mutants associated with familial cardiomyopathies.
|
18606848 |
2008 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
CLINVAR |
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
|
18646565 |
2007 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.
|
16061563 |
2005 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy.
|
15140538 |
2004 |
|
Cardiomyopathy, Familial Idiopathic
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.
|
15372542 |
2004 |