Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome

被引：640

作者：

Chavanas, S

Bodemer, C

Rochat, A

Hamel-Teillac, D

Ali, M

Irvine, AD

Bonafé, JL

Wilkinson, J

Taïeb, A

Barrandon, Y

Harper, JI

de Prost, Y

Hovnanian, A ^{[1
]}

机构：

[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England

[2] Necker Hosp, Dept Dermatol, Paris, France

[3] Ecole Normale Super, Epithelial Differentiat Lab, F-75231 Paris, France

[4] Amersham Hosp, Dept Dermatol, Amersham, England

[5] Great Ormond St Hosp Children, Dept Paediat Dermatol, London WC1N 3JH, England

[6] Rangueil Hosp, Dept Dermatol, Toulouse, France

[7] St Andre Hosp, Dept Dermatol, Bordeaux, France

来源：

NATURE GENETICS | 2000年 / 25卷 / 02期

关键词：

D O I：

10.1038/75977

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：141 / 142

页数：2

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