Clinical and genetic heterogeneity in laminopathies

Autosomal recessive LMNA mutation causing Restrictive Dermopathy

(2010) GJ Youn et al.   CLINICAL GENETICS

Modifier locus of the skeletal muscle involvement in Emery–Dreifuss muscular dystrophy

(2010) B. Granger et al.   HUMAN GENETICS

Laminopathies and lamin-associated signaling pathways

(2010) Nadir M. Maraldi et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Atypical Progeroid Syndrome due to Heterozygous MissenseLMNAMutations

(2009) Abhimanyu Garg et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation inLMNAAssociated to Charcot-Marie-Tooth Subtype CMT2B1 in Families from North Western Africa

(2008) T. Hamadouche et al.   ANNALS OF HUMAN GENETICS

De novoLMNAmutations cause a new form of congenital muscular dystrophy

(2008) Susana Quijano-Roy et al.   ANNALS OF NEUROLOGY

Severe Mandibuloacral Dysplasia-Associated Lipodystrophy and Progeria in a Young Girl with a Novel Homozygous Arg527CysLMNAMutation

(2008) Anil K. Agarwal et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

The Supramolecular Organization of the C. elegans Nuclear Lamin Filament

(2008) Kfir Ben-Harush et al.   JOURNAL OF MOLECULAR BIOLOGY

HGPS and related premature aging disorders: From genomic identification to the first therapeutic approaches

(2008) Sandrine Pereira et al.   MECHANISMS OF AGEING AND DEVELOPMENT

Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation

(2008) Nicola Carboni et al.   NEUROMUSCULAR DISORDERS