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X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay.
Rossanti, Rini; Nozu, Kandai; Fukunaga, Atsushi; Nagano, China; Horinouchi, Tomoko; Yamamura, Tomohiko; Sakakibara, Nana; Minamikawa, Shogo; Ishiko, Shinya; Aoto, Yuya; Okada, Eri; Ninchoji, Takeshi; Kato, Noritoshi; Maruyama, Shoichi; Kono, Keiji; Nishi, Shinichi; Iijima, Kazumoto; Fujii, Hideki.
  • Rossanti R; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan. riniariyadi@gmail.com.
  • Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Fukunaga A; Division of Dermatology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nagano C; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Horinouchi T; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Yamamura T; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Sakakibara N; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Minamikawa S; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Ishiko S; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Aoto Y; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Okada E; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Ninchoji T; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Kato N; Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Maruyama S; Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Kono K; Department of Nephrology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Nishi S; Department of Nephrology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Fujii H; Department of Nephrology, Kobe University Graduate School of Medicine, Kobe, Japan.
Clin Exp Nephrol ; 25(11): 1224-1230, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34128148

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Alfa-Galactosidasa / Cromosomas Humanos X / Inactivación del Cromosoma X Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Alfa-Galactosidasa / Cromosomas Humanos X / Inactivación del Cromosoma X Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Año: 2021 Tipo del documento: Article