Your browser doesn't support javascript.
loading
In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy.
Nishino, Tsubasa; Kobayashi, Akira; Mori, Natsuko; Masaki, Toshinori; Yokogawa, Hideaki; Fujiki, Keiko; Yanagawa, Ai; Murakami, Akira; Sugiyama, Kazuhisa.
Afiliación
  • Nishino T; Department of Ophthalmology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8641, Japan.
  • Kobayashi A; Department of Ophthalmology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8641, Japan. eyekoba@gmail.com.
  • Mori N; Department of Ophthalmology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8641, Japan.
  • Masaki T; Department of Ophthalmology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8641, Japan.
  • Yokogawa H; Department of Ophthalmology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8641, Japan.
  • Fujiki K; Department of Ophthalmology, Juntendo University Graduate School of Medical Science, Tokyo, Japan.
  • Yanagawa A; Department of Ophthalmology, Juntendo University Graduate School of Medical Science, Tokyo, Japan.
  • Murakami A; Department of Ophthalmology, Juntendo University Graduate School of Medical Science, Tokyo, Japan.
  • Sugiyama K; Department of Ophthalmology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8641, Japan.
Jpn J Ophthalmol ; 63(1): 46-55, 2019 Jan.
Article en En | MEDLINE | ID: mdl-30535821
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ADN / Epitelio Corneal / Distrofia Corneal Epitelial Juvenil de Meesmann / Queratina-12 / Mutación Tipo de estudio: Observational_studies Idioma: En Revista: Jpn J Ophthalmol Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ADN / Epitelio Corneal / Distrofia Corneal Epitelial Juvenil de Meesmann / Queratina-12 / Mutación Tipo de estudio: Observational_studies Idioma: En Revista: Jpn J Ophthalmol Año: 2019 Tipo del documento: Article