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Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels. [electronic resource] by
- Walter, C
- Gootjes, J
- Mooijer, P A
- Portsteffen, H
- Klein, C
- Waterham, H R
- Barth, P G
- Epplen, J T
- Kunau, W H
- Wanders, R J
- Dodt, G
Producer: 20010802
In:
American journal of human genetics vol. 69
Availability: No items available.
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9.
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Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis. [electronic resource] by
- van Grunsven, E G
- van Berkel, E
- Mooijer, P A
- Watkins, P A
- Moser, H W
- Suzuki, Y
- Jiang, L L
- Hashimoto, T
- Hoefler, G
- Adamski, J
- Wanders, R J
Producer: 19990310
In:
American journal of human genetics vol. 64
Availability: No items available.
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10.
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L-2-Hydroxyglutaric aciduria: normal L-2-hydroxyglutarate dehydrogenase activity in liver from two new patients. [electronic resource] by
- Wanders, R J
- Vilarinho, L
- Hartung, H P
- Hoffmann, G F
- Mooijer, P A
- Jansen, G A
- Huijmans, J G
- de Klerk, J B
- ten Brink, H J
- Jakobs, C
- Duran, M
Producer: 19971106
In:
Journal of inherited metabolic disease vol. 20
Availability: No items available.
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