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Renal complications in 6p duplication syndrome: Microarray‐based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)
Authors:Megumi Yoshimura‐Furuhata  Akira Nishimura‐Tadaki  Yoshiro Amano  Takashi Ehara  Yuko Hamasaki  Masaki Muramatsu  Seiichiro Shishido  Atsushi Aikawa  Riku Hamada  Kenji Ishikura  Hiroshi Hataya  Yoshihiko Hidaka  Shunsuke Noda  Kenichi Koike  Keiko Wakui  Yoshimitsu Fukushima  Naomichi Matsumoto  Midori Awazu  Noriko Miyake  Tomoki Kosho
Affiliation:1. Department of Pediatrics, Nagano Red Cross Hospital, Nagano, Japan;2. Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan;3. Department of Human Genetics, Yokohama City Graduate School of Medicine, Yokohama, Japan;4. Department of Health and Sport Science, Graduate School of Health Sciences, Matsumoto University, Matsumoto, Japan;5. Department of Pediatric Nephrology, School of Medicine, Toho University, Tokyo, Japan;6. Department of Nephrology, School of Medicine, Toho University, Tokyo, Japan;7. Department of Nephrology, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan;8. Department of Medical Genetics, Shinshu University School of Medicine, Matsumoto, Japan;9. Department of Pediatrics, School of Medicine, Keio University, Tokyo, Japan
Abstract:
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