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Monika Zwerger et al.
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Nuclear damages and oxidative stress: new perspectives for laminopathies
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Arrhythmia-related workup in hereditary myopathies
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Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy
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Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement
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A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement
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Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy
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NEUROMUSCULAR DISORDERS (2009)
De novo LMNA mutations cause a new form of congenital muscular dystrophy
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Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
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EUROPEAN JOURNAL OF CELL BIOLOGY (2005)
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JOURNAL OF MOLECULAR MEDICINE-JMM (2005)
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
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LMNA mutations in atypical Werner's syndrome
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Clinical relevance of atrial fibrillation/flutter, stroke, pacemaker implant, and heart failure in Emery-Dreifuss muscular dystrophy - A long-term longitudinal study
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