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)
Megumi Yoshimura‐Furuhata(Shinshu University), Tomoki Kosho(Shinshu University), Masaki Muramatsu(Queen Mary University of London), Riku Hamada, Yoshihiko Hidaka(Shinshu University), Yoshiro Amano(Nagano Red Cross Hospital), Seiichiro Shishido(Toho University), Shunsuke Noda(Shinshu University), Takashi Ehara(Matsumoto University), Yuko Hamasaki(Toho University), Midori Awazu(Tokyo Metropolitan Ohtsuka Hospital), Yoshimitsu Fukushima(Saitama Children's Medical Center), Hiroshi Hataya(Japanese Society for Dialysis Therapy), Akira Nishimura‐Tadaki(Yokohama City University), Kenji Ishikura(Kitasato University), Naomichi Matsumoto(Yokohama City University), Kenichi Koike(Shinshu University), Atsushi Aikawa(Toho University), Keiko Wakui(Shinshu University), Noriko Miyake(National Center for Global Health and Medicine)
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