1. Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. Issue 4 (11th March 2014) Authors: Handley, Mark T.; Mégarbané, André; Meynert, Alison M.; Brown, Stephen; Freyer, Elisabeth; Taylor, Martin S.; Jackson, Ian J.; Aligianis, Irene A. Journal: Molecular genetics & genomic medicine Issue: Volume 2:Issue 4(2014:Jul.) Page Start: 319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗