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A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency. [electronic resource] by
- Valnot, I
- von Kleist-Retzow, J C
- Barrientos, A
- Gorbatyuk, M
- Taanman, J W
- Mehaye, B
- Rustin, P
- Tzagoloff, A
- Munnich, A
- Rötig, A
Producer: 20000623
In:
Human molecular genetics vol. 9
Availability: No items available.
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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure. [electronic resource] by
- de Lonlay, P
- Valnot, I
- Barrientos, A
- Gorbatyuk, M
- Tzagoloff, A
- Taanman, J W
- Benayoun, E
- Chrétien, D
- Kadhom, N
- Lombès, A
- de Baulny, H O
- Niaudet, P
- Munnich, A
- Rustin, P
- Rötig, A
Producer: 20010927
In:
Nature genetics vol. 29
Availability: No items available.
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