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Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.
Koyanagi, Yoshito; Akiyama, Masato; Nishiguchi, Koji M; Momozawa, Yukihide; Kamatani, Yoichiro; Takata, Sadaaki; Inai, Chihiro; Iwasaki, Yusuke; Kumano, Mikako; Murakami, Yusuke; Omodaka, Kazuko; Abe, Toshiaki; Komori, Shiori; Gao, Dan; Hirakata, Toshiaki; Kurata, Kentaro; Hosono, Katsuhiro; Ueno, Shinji; Hotta, Yoshihiro; Murakami, Akira; Terasaki, Hiroko; Wada, Yuko; Nakazawa, Toru; Ishibashi, Tatsuro; Ikeda, Yasuhiro; Kubo, Michiaki; Sonoda, Koh-Hei.
Afiliación
  • Koyanagi Y; Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Akiyama M; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Nishiguchi KM; Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Momozawa Y; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Kamatani Y; Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Takata S; Department of Advanced Ophthalmic Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Inai C; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Iwasaki Y; Laboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Kumano M; Kyoto-McGill International Collaborative School in Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Murakami Y; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Omodaka K; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Abe T; Laboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
  • Komori S; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Gao D; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Hirakata T; Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Kurata K; Division of Clinical Cell Therapy, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Hosono K; Department of Ophthalmology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Ueno S; Department of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Hotta Y; Department of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Murakami A; Department of Ophthalmology, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Terasaki H; Department of Ophthalmology, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Wada Y; Department of Ophthalmology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Nakazawa T; Department of Ophthalmology, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Ishibashi T; Department of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Ikeda Y; Department of Ophthalmology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kubo M; Yuko Wada Eye Clinic, Sendai, Japan.
  • Sonoda KH; Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
J Med Genet ; 56(10): 662-670, 2019 10.
Article en En | MEDLINE | ID: mdl-31213501
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Pueblo Asiatico / Síndromes de Usher Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: J Med Genet Año: 2019 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Pueblo Asiatico / Síndromes de Usher Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: J Med Genet Año: 2019 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido