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Identification of a novel PEX14 mutation in Zellweger syndrome. [electronic resource] by
- Huybrechts, S J
- Van Veldhoven, P P
- Hoffman, I
- Zeevaert, R
- de Vos, R
- Demaerel, P
- Brams, M
- Jaeken, J
- Fransen, M
- Cassiman, D
Producer: 20080811
In:
Journal of medical genetics vol. 45
Availability: No items available.
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Farnesylation of Pex19p is not essential for peroxisome biogenesis in yeast and mammalian cells. [electronic resource] by
- Vastiau, I M K
- Anthonio, E A
- Brams, M
- Brees, C
- Young, S G
- Van de Velde, S
- Wanders, R J A
- Mannaerts, G P
- Baes, M
- Van Veldhoven, P P
- Fransen, M
Producer: 20060919
In:
Cellular and molecular life sciences : CMLS vol. 63
Availability: No items available.
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