Genetic and clinical characteristics of skeletal and cardiac muscle in patients with lamin A/C gene mutations
Author:
Affiliation:
1. Department of Public Health; Clinical and Molecular Medicine; Multiple Sclerosis Centre, via Is Guadazzonis 2, 09100 Cagliari, University of Cagliari; Italy
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology
Reference110 articles.
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3. The carboxyl-terminal region common to lamins A and C contains a DNA binding domain;Stierle;Biochemistry,2003
4. Novel and recurrent mutations in lamin A/C in patients with Emery-Dreyfuss muscular dystrophy;Brown;Am J Med Genet,2001
5. The nuclear lamina and its functions in the nucleus;Gruenbaum;Int Rev Cytol,2003
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