Related references
Note: Only part of the references are listed.Inflammatory changes in infantile-onset LMNA-associated myopathy
Hirofumi Komaki et al.
NEUROMUSCULAR DISORDERS (2011)
Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy
Miia Holmstrom et al.
JOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE (2011)
Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication
L. Volpi et al.
NEUROMUSCULAR DISORDERS (2010)
The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy
Daniel Vega Moller et al.
EUROPEAN JOURNAL OF HEART FAILURE (2009)
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
S. Benedetti et al.
NEUROLOGY (2007)
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene
J. Peter van Tintelen et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2007)
Laminopathies: A wide spectrum of human diseases
Howard J. Worman et al.
EXPERIMENTAL CELL RESEARCH (2007)
Crystal structure of the human lamin a coil 2B dimer: Implications for the head-to-tail association of nuclear lamins
SV Strelkov et al.
JOURNAL OF MOLECULAR BIOLOGY (2004)
Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations
T Sanna et al.
EUROPEAN HEART JOURNAL (2003)
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy
AJ van der Kooi et al.
NEUROLOGY (2002)
Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene
A Garg et al.
AMERICAN JOURNAL OF MEDICINE (2002)
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy
MR di Barletta et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)