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Links from Protein

Items: 3

1.
Identification of Novel Mutations and Sequence Variation in the Zellweger Syndrome Spectrum of Peroxisome Biogenesis Disorders
Wing Yan Yik, Steven J. Steinberg, Ann B. Moser, Hugo W. Moser, Joseph G. Hacia
Hum Mutat. Author manuscript; available in PMC 2009 Mar 2.
Published in final edited form as: Hum Mutat. 2009 Mar; 30(3): E467–E480. doi: 10.1002/humu.20932
PMCID:
PMC2649967
AbstractArticlePDF–853K
2.
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
Kanji Okumoto, Nobuyuki Shimozawa, Atsusi Kawai, Shigehiko Tamura, Toshiro Tsukamoto, Takashi Osumi, Hugo Moser, Ronald J. A. Wanders, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki
Mol Cell Biol. 1998 Jul; 18(7): 4324–4336. doi: 10.1128/mcb.18.7.4324
PMCID:
PMC109016
AbstractArticlePDF–3.3M
3.
Peroxisome deficient invertebrate and vertebrate animal models
Paul P. Van Veldhoven, Myriam Baes
Front Physiol. 2013; 4: 335. Published online 2013 Nov 22. doi: 10.3389/fphys.2013.00335
PMCID:
PMC3837297
AbstractArticlePDF–1.0M

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