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Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
Kubota, Daiki; Gocho, Kiyoko; Akeo, Keiichiro; Kikuchi, Sachiko; Sugahara, Michitaka; Matsumoto, Celso Soiti; Shinoda, Kei; Mizota, Atsushi; Yamaki, Kunihiko; Takahashi, Hiroshi; Kameya, Shuhei.
Afiliação
  • Kubota D; Department of Ophthalmology, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.
  • Gocho K; Department of Ophthalmology, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.
  • Akeo K; Department of Ophthalmology, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.
  • Kikuchi S; Department of Ophthalmology, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.
  • Sugahara M; Inoue Eye Clinic, 4-3 Surugadai, Kanda, Chiyoda-ku, Tokyo, 101-0062, Japan.
  • Matsumoto CS; Sugahara Eye Clinic, 1-13-3, Minami-senju, Arakawa-ku, Tokyo, 116-0003, Japan.
  • Shinoda K; Department of Ophthalmology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan.
  • Mizota A; Department of Ophthalmology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan.
  • Yamaki K; Department of Ophthalmology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan.
  • Takahashi H; Department of Ophthalmology, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inzai, Chiba, 270-1694, Japan.
  • Kameya S; Department of Ophthalmology, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo, 113-8602, Japan.
Doc Ophthalmol ; 132(3): 233-43, 2016 06.
Article em En | MEDLINE | ID: mdl-27071392
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Doenças Retinianas / Oftalmopatias Hereditárias / Canais de Cloreto / Proteínas do Olho Tipo de estudo: Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Doc Ophthalmol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Doenças Retinianas / Oftalmopatias Hereditárias / Canais de Cloreto / Proteínas do Olho Tipo de estudo: Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Doc Ophthalmol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão