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

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 11期

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

页码：849 / 852

页数：4

共 23 条

[1] Alopecia universalis associated with a mutation in the human hairless gene [J].

Ahmad, W ;

Haque, WFU ;

Brancolini, V ;

Tsou, HC ;

Haque, SU ;

Lam, H ;

Aita, VM ;

Owen, J ;

deBlaquiere, M ;

Frank, J ;

Cserhalmi-Friedman, PB ;

Leask, A ;

McGrath, JA ;

Peacocke, M ;

Ahmad, M ;

Ott, J ;

Christiano, AM .

SCIENCE, 1998, 279 (5351) :720-724

[2] Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping [J].

Chavanas, S ;

Garner, C ;

Bodemer, C ;

Ali, M ;

Hamel-Teillac, D ;

Wilkinson, J ;

Bonafé, JL ;

Paradisi, M ;

Kelsell, DP ;

Ansai, S ;

Mitsuhashi, Y ;

Larrègue, M ;

Leigh, IM ;

Harper, JI ;

Taïeb, A ;

de Prost, Y ;

Cardon, LR ;

Hovnanian, A .

AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (03) :914-921

[3] Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia [J].

Cichon, S ;

Anker, M ;

Vogt, IR ;

Rohleder, H ;

Pützstück, M ;

Hillmer, A ;

Farooq, SA ;

Al-Dhafri, KS ;

Ahmad, M ;

Haque, S ;

Rietschel, M ;

Propping, P ;

Kruse, R ;

Nöthen, MM .

HUMAN MOLECULAR GENETICS, 1998, 7 (11) :1671-1679

[4]

COTTINGHAM RW, 1993, AM J HUM GENET, V53, P252

[5]

FREIMER NB, 1993, AM J HUM GENET, V52, P1102

[6] Allegro, a new computer program for multipoint linkage analysis [J].

Gudbjartsson, DF ;

Jonasson, K ;

Frigge, ML ;

Kong, A .

NATURE GENETICS, 2000, 25 (01) :12-13

[7] THE SECRET LIFE OF THE HAIR FOLLICLE [J].

HARDY, MH .

TRENDS IN GENETICS, 1992, 8 (02) :55-61

[8] MENKES SYNDROME - AN UPDATED REVIEW [J].

HART, DB .

JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1983, 9 (01) :145-152

[9] Hair on a gene string: recent advances in understanding the molecular genetics of hair loss [J].

Irvine, AD ;

Christiano, AM .

CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2001, 26 (01) :59-71

[10] Desmoglein 4 in hair follicle differentiation and epidermal adhesion: Evidence from inherited hypotrichosis and acquired pemphigus vulgaris [J].

Kljuic, A ;

Bazzi, H ;

Sundberg, JP ;

Martinez-Mir, A ;

O'Shaughnessy, R ;

Mahoney, MG ;

Levy, M ;

Montagutelli, X ;

Ahmad, W ;

Alta, VM ;

Gordon, D ;

Uitto, J ;

Whiting, D ;

Ott, J ;

Fischer, S ;

Gilliam, TC ;

Jahoda, CAB ;

Morris, RJ ;

Panteleyev, AA ;

Nguyen, VT ;

Christiano, AM .

CELL, 2003, 113 (02) :249-260

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