Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array

• Mayuko Tamura,

  Affiliation Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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• Tsuyoshi Isojima,

  Affiliation Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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• Minae Kawashima,

  Affiliation Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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• Hideki Yoshida,

  Affiliation Department of Pediatrics, North Medical Center, Kyoto Prefectural University of Medicine, Kyoto, Japan

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• Keiko Yamamoto,

  Affiliation Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan

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• Taichi Kitaoka,

  Affiliation Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan

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• Noriyuki Namba,

  Affiliation Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan

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• Akira Oka,

  Affiliation Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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• Keiichi Ozono,

  Affiliation Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan

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• Katsushi Tokunaga,

  Affiliation Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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• Sachiko Kitanaka

  * E-mail: sachi-tky@umin.ac.jp

  Affiliation Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

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