1. Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome. Issue 8 (30th July 2004) Authors: Plasilova, M; Chattopadhyay, C; Pal, P; Schaub, N A; Buechner, S A; Mueller, Hj; Miny, P; Ghosh, A; Heinimann, K Journal: Journal of medical genetics Issue: Volume 41:Issue 8(2004) Page Start: 609 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗