Glycine substitution mutations by different amino acids at the same codon in COL7A1 cause different modes of dystrophic epidermolysis bullosa inheritance

被引：5

作者：

Sawamura, D.

Mochitomi, Y.

Kanzaki, T.

Nakamura, H.

Shimizu, H.

机构：

[1] Hokkaido Univ, Grad Sch Med, Kita Ku, Sapporo, Hokkaido 0608638, Japan

[2] Kagoshima Univ, Dept Dermatol, Grad Sch Med & Dent Sci, Kagoshima 890, Japan

来源：

BRITISH JOURNAL OF DERMATOLOGY | 2006年 / 155卷 / 04期

关键词：

COL7A1; collagen; dominant; dystrophic epidermolysis bullosa; recessive; type VII collagen;

D O I：

10.1111/j.1365-2133.2006.07388.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

[No abstract available]

引用

页码：834 / 837

页数：4

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