“…Mutations in the genes encoding lamin A and its binding partners have been associated with a variety of human diseases including Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy, limb girdle muscular dystrophy, Dunnigan-type familial partial lipodystrophy and Hutchinson-Gilford progeria syndrome (Bonne et al, 1999;Cao and Hegele, 2000;Eriksson et al, 2003;Fatkin et al, 1999;Muchir et al, 2000). Lamin A/C deficiency and other kinds of mutation may considerably alter the nuclear lamina, jeopardizing the structural integrity of the nucleus (Fidzianska et al, 1998;Hutchison et al, 2001;Lammerding et al, 2004Lammerding et al, , 2005Worman and Courvalin, 2004;Wilson, 2005).…”