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Results:
1-7
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Results: 7
Authors:
Pequignot, MO
Dey, R
Zeviani, M
Tiranti, V
Godinot, C
Poyau, A
Sue, C
Di Mauro, S
Abitbol, M
Marsac, C
Citation: Mo. Pequignot et al., Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase deficiency, HUM MUTAT, 17(5), 2001, pp. 374-381
Authors:
Legros, F
Chatzoglou, E
Frachon, P
de Baulny, HO
Laforet, P
Jardel, C
Godinot, C
Lombes, A
Citation: F. Legros et al., Functional characterization of novel mutations in the human cytochrome b gene, EUR J HUM G, 9(7), 2001, pp. 510-518
Authors:
Liu, JB
Wang, CS
Murakami, Y
Gong, GG
Ishibashi, Y
Prody, C
Ochiai, K
Bache, RJ
Godinot, C
Zhang, JY
Citation: Jb. Liu et al., Mitochondrial ATPase and high-energy phosphates in failing hearts, AM J P-HEAR, 281(3), 2001, pp. H1319-H1326
Authors:
Carrier, H
Flocard, F
Tagliati, V
Arrigo, AP
Godinot, C
Citation: H. Carrier et al., Immunolabelling of mitochondrial superoxide dismutase and of Hsp60 in muscles harbouring a respiratory chain deficiency, NEUROMUSC D, 10(2), 2000, pp. 144-149
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
Authors:
Drouet, A
Guilloton, L
Godinot, C
Rochet, D
Ribot, C
Carrier, H
Citation: A. Drouet et al., Complicated diabetes-deafness syndrome or association with a MELAS syndrome, in a patient harboring the mitochondrial DNA mutation at position 3243?, REV NEUROL, 156(10), 2000, pp. 892-895
Authors:
Poyau, A
Buchet, K
Godinot, C
Citation: A. Poyau et al., Sequence conservation from human to prokaryotes of Surf1, a protein involved in cytochrome c oxidase assembly, deficient in Leigh syndrome, FEBS LETTER, 462(3), 1999, pp. 416-420
Risultati:
1-7
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