✦ LIBER ✦

Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13

✍ Scribed by Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; Atsushi Imamura; Toshiro Tsukamoto; Takashi Osumi; Keita Tateishi; Kanji Okumoto; Yukio Fujiki; Tadao Orii; Peter G. Barth; Ronald J.A. Wanders; Naomi Kondo

Book ID: 115581537
Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 671 KB
Volume: 243
Category: Article
ISSN: 0006-291X
DOI: 10.1006/bbrc.1997.8067

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Identification of a new complementation

Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene

✍ Nobuyuki Shimozawa; Toshiro Tsukamoto; Tomoko Nagase; Yasuhiko Takemoto; Naoki K 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 292 KB

## Communicated by Jean-Louis Mandel Peroxisome biogenesis disorders (PBD) are lethal hereditary diseases caused by abnormalities in the biogenesis of peroxisomes. At present, 12 different complementation groups have been identified and to date, all genes responsible for each of these complementat

Genetic Basis of Peroxisome-Assembly Mut

Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts

✍ Nobuyuki Shimozawa; Yasuyuki Suzuki; Zhongyi Zhang; Atsushi Imamura; Naomi Kondo 📂 Article 📅 1998 🏛 American Society of Human Genetics 🌐 English ⚖ 405 KB