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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