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

被引：100

作者：

Yamamoto, S

Okada, M

Tsujikawa, M

Shimomura, Y

Nishida, K

Inoue, Y

Watanabe, H

Maeda, N

Kurahashi, H

Kinoshita, S

Nakamura, Y

Tano, Y

机构：

[1] Osaka Univ, Sch Med, Dept Ophthalmol, Suita, Osaka 565, Japan

[2] Osaka Univ, Sch Med, Dept Clin Genet, Suita, Osaka 565, Japan

[3] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kyoto, Japan

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 62卷 / 03期

关键词：

D O I：

10.1086/301765

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：719 / 722

页数：4

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