1. Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency. Issue 12 (18th December 2003) Authors: Lebon, S; Chol, M; Benit, P; Mugnier, C; Chretien, D; Giurgea, I; Kern, I; Girardin, E; Hertz-Pannier, L; de Lonlay, P; Rötig, A; Rustin, P; Munnich, A Journal: Journal of medical genetics Issue: Volume 40:Issue 12(2003) Page Start: 896 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗