Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes

• Minoru Nakayama,

  Affiliations Genome and Drug Research Center, Tokyo University of Science, Noda, Chiba, Japan, Department of Biological Science and Technology, Tokyo University of Science, Noda, Chiba, Japan, Research Institute for Science and Technology, Tokyo University of Science, Noda, Chiba, Japan

  ⨯
• Hiroyasu Sato,

  Affiliation Department of Biological Science and Technology, Tokyo University of Science, Noda, Chiba, Japan

  ⨯
• Takayuki Okuda,

  Affiliation Department of Biological Science and Technology, Tokyo University of Science, Noda, Chiba, Japan

  ⨯
• Nao Fujisawa,

  Affiliation Department of Biological Science and Technology, Tokyo University of Science, Noda, Chiba, Japan

  ⨯
• Nozomu Kono,

  Affiliation Graduate School of Pharmaceutical Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan

  ⨯
• Hiroyuki Arai,

  Affiliation Graduate School of Pharmaceutical Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan

  ⨯
• Emiko Suzuki,

  Affiliation Structural Biology Center, National Institute of Genetics, and Department of Genetics, The Graduate University for Advanced Studies, Mishima, Shizuoka, Japan

  ⨯
• Masato Umeda,

  Affiliation Institute for Chemical Research, Kyoto University, Uji, Kyoto, Japan

  ⨯
• Hiroyuki O. Ishikawa,

  Affiliation Genome and Drug Research Center, Tokyo University of Science, Noda, Chiba, Japan

  ⨯
• Kenji Matsuno

  * E-mail: matsuno@rs.noda.tus.ac.jp

  Affiliations Genome and Drug Research Center, Tokyo University of Science, Noda, Chiba, Japan, Department of Biological Science and Technology, Tokyo University of Science, Noda, Chiba, Japan, Research Institute for Science and Technology, Tokyo University of Science, Noda, Chiba, Japan

  ⨯