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Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects
Authors:Håkelien Anne-Mari  Delbarre Erwan  Gaustad Kristine G  Buendia Brigitte  Collas Philippe
Affiliation:Institute of Basic Medical Sciences, Department of Biochemistry, Faculty of Medicine, University of Oslo, PO Box 1112 Blindern, 0317 Oslo, Norway.
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