Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome. Issue 8 (30th July 2004) - Plasilova, M; Chattopadhyay, C; Pal, P; Schaub, N A; Buechner, S A; Mueller, Hj; Miny, P; Ghosh, A; Heinimann, K