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

doi:10.1086/301765

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

Research output: Contribution to journal › Letter

96 Citations (Scopus)

Original language	English
Pages (from-to)	719-722
Number of pages	4
Journal	American Journal of Human Genetics
Volume	62
Issue number	3
DOIs	https://doi.org/10.1086/301765
Publication status	Published - 01-01-1998
Externally published	Yes

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

Cite this

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

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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.

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.

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AU - Nishida, K.

AU - Inoue, Y.

AU - Watanabe, H.

AU - Maeda, N.

AU - Kurahashi, H.

AU - Kinoshita, S.

AU - Nakamura, Y.

AU - Tano, Y.

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10.1086/301765