Fig. 1From: An alpha-helix variant p.Arg156Pro in LMNA as a cause of hereditary dilated cardiomyopathy: genetics and bioinfomatics exploration(A) The structure of lamin A/C. (B) The wild type α-Helix structure in object region. (C) The pathongenic α-Helix variant of lamin A/C-p.Arg156Pro(LMNA-c.467G > C)Back to article page