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Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

Arimura, T and Helbling-Leclerc, A and Varnous, S and Niel, F and Lacene, E and Fromes, Y and Toussaint, M and Mura, A M and Keller, D I and Amthor, H and Isnard, R and Malissen, M and Schwartz, K and Bonne, G (2005) Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. HUMAN MOLECULAR GENETICS, 14 (1). pp. 155-169.

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Item Type: Article
RVC Publication Type: Research (full) paper
WoS ID: 000226199300015
DOI: https://doi.org/10.1093/hmg/ddi017
Departments: Comparative Biomedical Sciences
Depositing User: RVC Auto-import
Date Deposited: 11 Nov 2014 18:45
Last Modified: 20 Aug 2016 05:00
URI: http://researchonline.rvc.ac.uk/id/eprint/783