Volume 11, Issue S1 pp. S278-S283
Mutation in Brief
Free Access

Mutational analyses of AVPR2 gene in three Japanese families with X-linked nephrogenic diabetes insipidus: Two recurrent mutations, R137H and ΔV278, caused by the hypermutability at CpG dinucleotides

Yutaka Shoji M.D.

Corresponding Author

Yutaka Shoji M.D.

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

Department of Pediatrics, Akita University School of Medicine, Hondo 1-1-1, Akita-shi, Akita 010 JapanSearch for more papers by this author
Tsutomu Takahashi

Tsutomu Takahashi

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

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Yukiko Suzuki

Yukiko Suzuki

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

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Takashi Suzuki

Takashi Suzuki

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

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Kazuo Komatsu

Kazuo Komatsu

Department of Pediatrics, Yuri General Hospital, Akita, Japan

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Hiyoshi Hirono

Hiyoshi Hirono

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

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Yasuko Shoji

Yasuko Shoji

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

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Takehiko Yokoyama

Takehiko Yokoyama

Department of Pediatrics, Seirei Hamamatsu General Hospital, Shizuoka, Japan

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Hideyuki Kito

Hideyuki Kito

Department of Pediatrics, Seirei Hamamatsu General Hospital, Shizuoka, Japan

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Goro Takada

Goro Takada

Department of Pediatrics, Akita University School of Medicine, Akita, Japan

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First published: 28 April 2011
Citations: 10
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