Results
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501.
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502.
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A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents. [electronic resource] by
- Raas-Rothschild, Annick
- Wanders, Ronald J A
- Mooijer, Petra A W
- Gootjes, Jeannette
- Waterham, Hans R
- Gutman, Alisa
- Suzuki, Yasuyuki
- Shimozawa, Nobuyuki
- Kondo, Naomi
- Eshel, Gideon
- Espeel, Marc
- Roels, Frank
- Korman, Stanley H
Producer: 20020418
In:
American journal of human genetics vol. 70
Availability: No items available.
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503.
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PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p. [electronic resource] by
- Okumoto, K
- Shimozawa, N
- Kawai, A
- Tamura, S
- Tsukamoto, T
- Osumi, T
- Moser, H
- Wanders, R J
- Suzuki, Y
- Kondo, N
- Fujiki, Y
Producer: 19980716
In:
Molecular and cellular biology vol. 18
Availability: No items available.
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504.
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Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies. [electronic resource] by
- Funato, Michinori
- Shimozawa, Nobuyuki
- Nagase, Tomoko
- Takemoto, Yasuhiko
- Suzuki, Yasuyuki
- Imamura, Yoshihiko
- Matsumoto, Tadashi
- Tsukamoto, Toshiro
- Kojidani, Tomoko
- Osumi, Takashi
- Fukao, Toshiyuki
- Kondo, Naomi
Producer: 20060726
In:
Brain & development vol. 28
Availability: No items available.
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505.
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506.
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507.
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508.
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509.
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510.
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511.
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512.
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513.
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514.
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515.
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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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516.
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517.
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518.
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519.
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520.
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