Disentangling the roots of inherited hair disorders

被引：7
|
作者：
Sprecher, Eli
机构：
[1] Technion Israel Inst Technol, Fac Med, Dept Dermatol, Lab Mol Dermatol, IL-31096 Haifa, Israel
[2] Technion Israel Inst Technol, Fac Med, Rappaport Inst, IL-31096 Haifa, Israel
来源：
NATURE GENETICS | 2008年 / 40卷 / 03期
关键词：
D O I：
10.1038/ng0308-265
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
Rare syndromes offer unique opportunities to gain insight into central physiological processes. By deciphering the genetic basis of two rare inherited diseases, two studies identify a key role for P2Y5, a G protein-coupled receptor, in hair follicle development.
引用
收藏
页码：265 / 266
页数：2
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