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 journalLetter

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

Fingerprint

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.
@article{0261b6a42ab94425be4cb3d0e72a99f4,
title = "A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA [4]",
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 Hiroki Kurahashi and S. Kinoshita and Y. Nakamura and Y. Tano",
year = "1998",
month = "1",
day = "1",
doi = "10.1086/301765",
language = "English",
volume = "62",
pages = "719--722",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "3",

}

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 journalLetter

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

UR - http://www.scopus.com/inward/record.url?scp=17744411573&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=17744411573&partnerID=8YFLogxK

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