Laminopathies: Multisystem dystrophy syndromes
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference96 articles.
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3. A homozygous mutation in the Lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis and progeroid features;Van Esch;J. Clin. Endocrinol. Metabol.,2005
4. Nuclear lamins: their structure, assembly, and interactions;Stuurman;J. Struct. Biol.,1998
5. Lamin expression in human adipose cells in relation to anatomical site and differentiation state;Lelliott;J. Clin. Endocrinol. Metab.,2002
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