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, Hiroki Kurahashi, S. Kinoshita, Y. Nakamura, Y. Tano

Research output: Contribution to journal › Letter

95 Citations (Scopus)
Original languageEnglish
Pages (from-to)719-722
Number of pages4
JournalAmerican Journal of Human Genetics
Volume62
Issue number3
DOIs
Publication statusPublished - 01-01-1998

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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)

Cite this

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, Hiroki ; Kinoshita, S. ; Nakamura, Y. ; Tano, Y. / A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]. In: American Journal of Human Genetics. 1998 ; Vol. 62, No. 3. pp. 719-722.
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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, vol. 62, no. 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, Hiroki; Kinoshita, S.; Nakamura, Y.; Tano, Y.

In: American Journal of Human Genetics, Vol. 62, No. 3, 01.01.1998, p. 719-722.

Research output: Contribution to journal › 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, Hiroki

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

IS - 3

ER -

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

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