Related references
Note: Only part of the references are listed.MUSCLE IMAGING ANALOGIES IN A COHORT OF PATIENTS WITH DIFFERENT CLINICAL PHENOTYPES CAUSED BY LMNA GENE MUTATIONS
Nicola Carboni et al.
MUSCLE & NERVE (2010)
Lamin A/C deficiency as a cause of familial dilated cardiomyopathy
Rohit Malhotra et al.
CURRENT OPINION IN CARDIOLOGY (2009)
Long-term outcome and risk stratification in dilated cardiolaminopathies
Michele Pasotti et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2008)
Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation
Nicola Carboni et al.
NEUROMUSCULAR DISORDERS (2008)
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
S. Benedetti et al.
NEUROLOGY (2007)
Laminopathies: Multisystem dystrophy syndromes
KN Jacob et al.
MOLECULAR GENETICS AND METABOLISM (2006)
Primary prevention of sudden death in patients with lamin A/C gene mutations
C Meune et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
LMNA mutation position predicts organ system involvement in laminopathies
RA Hegele
CLINICAL GENETICS (2005)
Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?
JH van Berlo et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2005)
p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria
J Kirschner et al.
ANNALS OF NEUROLOGY (2005)
A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia
C Goizet et al.
JOURNAL OF MEDICAL GENETICS (2004)
The carboxyl-terminal region common to lamins A and C contains a DNA binding domain
VN Stierlé et al.
BIOCHEMISTRY (2003)
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy
AJ van der Kooi et al.
NEUROLOGY (2002)
Life at the edge: The nuclear envelope and human disease
B Burke et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2002)
Molecular characterization of protein kinase C-alpha binding to lamin A
AM Martelli et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2002)
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy
CA Brown et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2001)
Transcriptional repression, apoptosis, human disease and the functional evolution of the nuclear lamina
M Cohen et al.
TRENDS IN BIOCHEMICAL SCIENCES (2001)
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)
Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement
GL Brodsky et al.
CIRCULATION (2000)
Share Paper
