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Glycosylphosphatidylinositol (GPI) anchor deficiency caused by mutations in PIGW is associated with West syndrome and hyperphosphatasia with mental retardation syndrome

Authors

  • Tomohiro Chiyonobu Department of Pediatrics, Kyoto Prefectural University of Medicine, Kamigyo, Kyoto, Japan PubMed articlesGoogle scholar articles
  • Norimitsu Inoue Department of Molecular Genetics, Osaka Medical Center for Cancer, Osaka, Japan PubMed articlesGoogle scholar articles
  • Masafumi Morimoto Department of Pediatrics, Kyoto Prefectural University of Medicine, Kamigyo, Kyoto, Japan PubMed articlesGoogle scholar articles
  • Taroh Kinoshita Department of Immunoregulation, Research Institute for Microbial Diseases, Suita, Osaka, Japan Laboratory of Immunoglycobiology, WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan PubMed articlesGoogle scholar articles
  • Yoshiko Murakami Department of Immunoregulation, Research Institute for Microbial Diseases, Suita, Osaka, Japan Laboratory of Immunoglycobiology, WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Yoshiko Murakami, Department of Immunoregulation Research Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan; yoshiko{at}biken.osaka-u.ac.jp
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Citation

Chiyonobu T, Inoue N, Morimoto M, et al
Glycosylphosphatidylinositol (GPI) anchor deficiency caused by mutations in PIGW is associated with West syndrome and hyperphosphatasia with mental retardation syndrome

Publication history

  • Received November 6, 2013
  • Revised December 2, 2013
  • Accepted December 3, 2013
  • First published December 23, 2013.
Online issue publication 
February 14, 2014

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