A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2:: an RNA-based genetic analysis using a single hair bulb

被引：4
|
作者：
Tsuda, T. [1 ]
Ishikawa, C. [1 ]
Nakagawa, N. [1 ]
Konishi, H. [1 ]
Tarutani, M. [1 ]
Matsuki, M. [1 ]
Yamanishi, K. [1 ]
机构：
[1] Hyogo Med Univ, Dept Dermatol, Nishinomiya, Hyogo 6638501, Japan
来源：
BRITISH JOURNAL OF DERMATOLOGY | 2008年 / 159卷 / 03期
关键词：
hair bulb; keratin; 17; pachyonychia congenita; point mutation; RNA;
D O I：
10.1111/j.1365-2133.2008.08684.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
收藏
页码：730 / 732
页数：3
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