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Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. [electronic resource] by
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- Hashiguchi, N
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- Masuno, M
- Imaizumi, K
- Kuroki, Y
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- Orii, T
- Kondo, N
Producer: 19970114
In:
American journal of human genetics vol. 59
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562.
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Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders. [electronic resource] by
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- Suzuki, Y
- Zhang, Z
- Imamura, A
- Toyama, R
- Mukai, S
- Fujiki, Y
- Tsukamoto, T
- Osumi, T
- Orii, T
- Wanders, R J
- Kondo, N
Producer: 19990708
In:
Human molecular genetics vol. 8
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575.
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Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals. [electronic resource] by
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- Imanaka, T
- Okumoto, K
- Suzuki, Y
- Kondo, N
- Fujiki, Y
Producer: 19981013
In:
The Journal of biological chemistry vol. 273
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A mouse model for Zellweger syndrome. [electronic resource] by
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- Fransen, M
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- Declercq, P E
- Collen, D
- van Veldhoven, P P
- Mannaerts, G P
Producer: 19971002
In:
Nature genetics vol. 17
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580.
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