rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathies.
|
22266370 |
2012 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.
|
23853504 |
2013 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Limb-girdle muscular dystrophy with severe heart failure overlapping with lipodystrophy in a patient with LMNA mutation p.Ser334del.
|
27585670 |
2017 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
|
23183350 |
2013 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Genetic testing for dilated cardiomyopathy in clinical practice.
|
22464770 |
2012 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.
|
29149195 |
2017 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Lamin A/C mutations in dilated cardiomyopathy.
|
24846508 |
2014 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.
|
29237675 |
2017 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly.
|
27723096 |
2017 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs386134243
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy.
|
22224630 |
2012 |