3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population

被引：34

作者：

Vavassori, P ^{[1
]}

Borgiani, P

D'Apice, MR

De Nigris, F

Blanco, GD

Monteleone, I

Biancone, L

Novelli, G

Pallone, F

机构：

[1] Univ Roma Tor Vergata, Gastroenterol Unit, Ctr Eccelenza Studio Rischio Genom Patol Compless, Rome, Italy

[2] Univ Roma Tor Vergata, Genet Unit, Ctr Eccelenza Studio Rischio Genom Patol Compless, Rome, Italy

来源：

DIGESTIVE AND LIVER DISEASE | 2002年 / 34卷 / 02期

关键词：

D O I：

10.1016/S1590-8658(02)80249-3

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

引用

页码：153 / 153

页数：1

共 3 条

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[2] Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease [J].

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NATURE, 2001, 411 (6837) :599-603

[3] A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease [J].

Ogura, Y ;

Bonen, DK ;

Inohara, N ;

Nicolae, DL ;

Chen, FF ;

Ramos, R ;

Britton, H ;

Moran, T ;

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Cho, JH .

NATURE, 2001, 411 (6837) :603-606

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