Authors:
Jaksch, M
Ogilvie, I
Yao, JB
Kortenhaus, G
Bresser, HG
Gerbitz, KD
Shoubridge, EA
Citation: M. Jaksch et al., Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency, HUM MOL GEN, 9(5), 2000, pp. 795-801
Authors:
Poyau, A
Buchet, K
Bouzidi, MF
Zabot, MT
Echenne, B
Yao, JB
Shoubridge, EA
Godinot, C
Citation: A. Poyau et al., Missense mutations in SURF1 associated with deficient cytochrome c oxidaseassembly in Leigh syndrome patients, HUM GENET, 106(2), 2000, pp. 194-205
Citation: Jb. Yao et al., The tribological performance of nematic liquid crystal 4-n-pentyl-4 '-cyanobiphenyl (5CB) as a lubricant additive((c)), LUBRIC ENG, 56(6), 2000, pp. 21-25
Authors:
Horvath, R
Lochmuller, H
Stucka, R
Yao, JB
Shoubridge, EA
Kim, SH
Gerbitz, KD
Jaksch, M
Citation: R. Horvath et al., Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency, BIOC BIOP R, 276(2), 2000, pp. 530-533
Citation: Jb. Yao et Ea. Shoubridge, Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency, HUM MOL GEN, 8(13), 1999, pp. 2541-2549