A missense mutation in the type II hair keratin hHb3 is associated with monilethrix

被引：57
|
作者：
van Steensel, MAM
Steijlen, PM
Bladergroen, RS
Vermeer, M
van Geel, M
机构：
[1] Univ Hosp Maastricht, Dept Dermatol, NL-6202 AZ Maastricht, Netherlands
[2] Univ Med Ctr Leiden, Dept Dermatol, Leiden, Netherlands
来源：
JOURNAL OF MEDICAL GENETICS | 2005年 / 42卷 / 03期
关键词：
D O I：
10.1136/jmg.2004.021030
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页数：4
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