×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
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
Monogenic diabetes
0.410
GeneticVariation
CLINVAR
Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.
23853504
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.
23853504
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
GeneticVariation
CLINVAR
Cosegregation of focal segmental glomerulosclerosis in a family with familial partial lipodystrophy due to a mutation in LMNA.
24080738
2013
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Phenotypic diversity in patients with lipodystrophy associated with LMNA mutations.
22700598
2012
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
GeneticVariation
CLINVAR
Genotype-phenotype correlations in laminopathies: how does fate translate?
20074070
2010
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
The role of LMNA in adipose: a novel mouse model of lipodystrophy based on the Dunnigan-type familial partial lipodystrophy mutation.
19201734
2009
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Laminopathies: multisystem dystrophy syndromes.
16364671
2006
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy.
16415042
2006
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
GeneticVariation
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
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Heterogeneity of nuclear lamin A mutations in Dunnigan-type familial partial lipodystrophy.
10999845
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
10655060
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Lamin A/C mutation in a woman and her two daughters with Dunnigan-type partial lipodystrophy and insulin resistance.
10868844
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.
10739751
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.
10587585
2000
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
CausalMutation
CLINVAR
Isolation and characterization of catalytic and calmodulin-binding domains of Bordetella pertussis adenylate cyclase.
2007407
1991
×
Entrez Id:
4000
Gene Symbol:
LMNA
LMNA
Monogenic diabetes
0.410
GeneticVariation
CLINVAR
Diagnostic validity of the MAST and the alcohol dependence scale in the assessment of DSM-III alcohol disorders.
2270059
1990