A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3

被引:29
作者
Aslam, M
Chahrour, MH
Razzaq, A
Haque, S
Yan, K
Leal, SM
Ahmad, W [1 ]
机构
[1] Quaid I Azam Univ, Dept Biol Sci, Islamabad, Pakistan
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
D O I
10.1136/jmg.2004.019729
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
页码:849 / 852
页数:4
相关论文
共 23 条
[21]   ISOLATION OF A CANDIDATE GENE FOR MENKES DISEASE AND EVIDENCE THAT IT ENCODES A COPPER-TRANSPORTING ATPASE [J].
VULPE, C ;
LEVINSON, B ;
WHITNEY, S ;
PACKMAN, S ;
GITSCHIER, J .
NATURE GENETICS, 1993, 3 (01) :7-13
[22]  
WEEKS DE, 1995, AM J HUM GENET, V56, P1506
[23]   A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix [J].
Winter, H ;
Rogers, MA ;
Gebhardt, M ;
Wollina, U ;
Boxall, L ;
Chitayat, D ;
BabulHirji, R ;
Stevens, HP ;
Zlotogorski, A ;
Schweizer, J .
HUMAN GENETICS, 1997, 101 (02) :165-169