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- Suzuki, Y
- Kumazaki, K
- Tanabe, Y
- Akaboshi, S
- Miura, K
- Shimozawa, N
- Kondo, N
- Nishiguchi, T
- Terada, K
- Orii, T
Producer: 19970319
In:
Epilepsia vol. 38
Availability: No items available.
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425.
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426.
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Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines. [electronic resource] by
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- Raymond, Gerald V
- Rizzo, William B
- Moser, Ann B
- Wilkinson, Mark E
- Stone, Edwin M
- Steinberg, Steven J
- Wangler, Michael F
- Rush, Eric T
- Hacia, Joseph G
- Bose, Mousumi
Producer: 20161213
In:
Molecular genetics and metabolism vol. 117
Availability: No items available.
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427.
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428.
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429.
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Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene. [electronic resource] by
- Shimozawa, Nobuyuki
- Tsukamoto, Toshiro
- Nagase, Tomoko
- Takemoto, Yasuhiko
- Koyama, Naoki
- Suzuki, Yasuyuki
- Komori, Masayuki
- Osumi, Takashi
- Jeannette, Gootjes
- Wanders, Ronald J A
- Kondo, Naomi
Producer: 20040924
In:
Human mutation vol. 23
Availability: No items available.
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430.
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431.
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432.
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433.
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438.
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A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome. [electronic resource] by
- Shimozawa, N
- Suzuki, Y
- Tomatsu, S
- Nakamura, H
- Kono, T
- Takada, H
- Tsukamoto, T
- Fujiki, Y
- Orii, T
- Kondo, N
Producer: 19990630
In:
Human mutation vol. Suppl 1
Availability: No items available.
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439.
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440.
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