A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]

S. Yamamoto, M. Okada, M. Tsujikawa, Y. Shimomura, K. Nishida, Y. Inoue, H. Watanabe, N. Maeda, H. Kurahashi, S. Kinoshita, Y. Nakamura, Y. Tano

研究成果: Letter

98 引用 (Scopus)
元の言語English
ページ(範囲)719-722
ページ数4
ジャーナルAmerican Journal of Human Genetics
62
発行部数3
DOI
出版物ステータスPublished - 01-01-1998
外部発表Yes

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

これを引用

Yamamoto, S., Okada, M., Tsujikawa, M., Shimomura, Y., Nishida, K., Inoue, Y., Watanabe, H., Maeda, N., Kurahashi, H., Kinoshita, S., Nakamura, Y., & Tano, Y. (1998). A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]. American Journal of Human Genetics, 62(3), 719-722. https://doi.org/10.1086/301765