Glycine substitution mutations by different amino acids in the same codon of COL7A1 lead to heterogeneous clinical phenotypes of dominant dystrophic epidermolysis bullosa

被引：0

作者：

T. Murata

T. Masunaga

H. Shimizu

Y. Takizawa

A Ishiko

N. Hatta

T. Nishikawa

机构：

[1] Department of Dermatology,

[2] Keio University School of Medicine,undefined

[3] 35 Shinanomachi,undefined

[4] Shinjuku,undefined

[5] Tokyo 160-8582,undefined

[6] Japan e-mail: takayuki@med.keio.ac.jp,undefined

[7] Tel.: +81-3-33531211,undefined

[8] Fax: +81-3-33516880,undefined

[9] Department of Dermatology,undefined

[10] Hokkaido University School of Medicine,undefined

[11] Sapporo,undefined

[12] Japan,undefined

[13] Department of Dermatology,undefined

[14] Kanazawa University School of Medicine,undefined

[15] Kanazawa,undefined

[16] Japan,undefined

来源：

Archives of Dermatological Research | 2000年 / 292卷

关键词：

Key words Type VII collagen; Pruriginosa; Anchoring fibril; Basement membrane;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：477 / 481

页数：4