Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling

(2013) Monika Zwerger et al.   HUMAN MOLECULAR GENETICS

Lamin A Δexon9 mutation leads to telomere and chromatin defects but not genomic instability

(2013) Arindam Das et al.   Nucleus

Lamins in development, tissue maintenance and stress

(2012) Noam Zuela et al.   EMBO REPORTS

Nuclear damages and oxidative stress: new perspectives for laminopathies

(2012) G. Lattanzi et al.   EUROPEAN JOURNAL OF HISTOCHEMISTRY

Arrhythmia-related workup in hereditary myopathies

(2012) Josef Finsterer et al.   JOURNAL OF ELECTROCARDIOLOGY

Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy

(2012) M. P. Menezes et al.   NEUROLOGY

A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement

(2012) Ayako Hattori et al.   NEUROMUSCULAR DISORDERS

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death

(2011) Anne T. Bertrand et al.   HUMAN MOLECULAR GENETICS

Nuclear lamins and laminopathies

(2011) Howard J. Worman   JOURNAL OF PATHOLOGY

Inflammatory changes in infantile-onset LMNA-associated myopathy

(2011) Hirofumi Komaki et al.   NEUROMUSCULAR DISORDERS

Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement

(2011) Christophe Meune et al.   NEUROMUSCULAR DISORDERS

The lamin protein family

(2011) Travis A Dittmer et al.   GENOME BIOLOGY

Gene expression, chromosome position and lamin A/C mutations

(2011) Megan J. Puckelwartz et al.   Nucleus

Laminopathies and lamin-associated signaling pathways

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

Two children with “dropped head” syndrome due to lamin A/C mutations

(2010) Jeremy C. Chemla et al.   MUSCLE & NERVE

De novoLMNAmutations cause a new form of congenital muscular dystrophy

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

Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy

(2008) Samira Makri et al.   NEUROMUSCULAR DISORDERS