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

95 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

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Neoplasm Proteins
Hereditary Corneal Dystrophies
Extracellular Matrix Proteins
Pedigree
Transforming Growth Factor beta
Mutation
betaIG-H3 protein
Lattice Type IIIA Corneal Dystrophy

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

A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]. / Yamamoto, S.; Okada, M.; Tsujikawa, M.; Shimomura, Y.; Nishida, K.; Inoue, Y.; Watanabe, H.; Maeda, N.; Kurahashi, H.; Kinoshita, S.; Nakamura, Y.; Tano, Y.

:: American Journal of Human Genetics, 巻 62, 番号 3, 01.01.1998, p. 719-722.

研究成果: Letter

TY - JOUR

T1 - A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]

AU - Yamamoto, S.

AU - Okada, M.

AU - Tsujikawa, M.

AU - Shimomura, Y.

AU - Nishida, K.

AU - Inoue, Y.

AU - Watanabe, H.

AU - Maeda, N.

AU - Kurahashi, H.

AU - Kinoshita, S.

AU - Nakamura, Y.

AU - Tano, Y.

PY - 1998/1/1

Y1 - 1998/1/1

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U2 - 10.1086/301765

DO - 10.1086/301765

M3 - Letter

C2 - 9497262

AN - SCOPUS:17744411573

VL - 62

SP - 719

EP - 722

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

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Yamamoto S, Okada M, Tsujikawa M, Shimomura Y, Nishida K, Inoue Y その他. A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]. American Journal of Human Genetics. 1998 1 1;62(3):719-722. https://doi.org/10.1086/301765