Association of X-prolyl aminopeptidase 1 rs17095355 polymorphism with biliary atresia in Thai children

被引：32

作者：

Kaewkiattiyot, Sarannut

Honsawek, Sittisak ^{[2
]}

Vejchapipat, Paisarn ^{[3
]}

Chongsrisawat, Voranush

Poovorawan, Yong ^{[1
]}

机构：

[1] Chulalongkorn Univ, Fac Med, Dept Pediat, Ctr Excellence Clin Virol, Bangkok 10330, Thailand

[2] Chulalongkorn Univ, Fac Med, Dept Biochem, Bangkok 10330, Thailand

[3] Chulalongkorn Univ, Fac Med, Dept Surg, Bangkok 10330, Thailand

来源：

HEPATOLOGY RESEARCH | 2011年 / 41卷 / 12期

关键词：

Biliary atresia; polymorphism; X-prolyl aminopeptidase 1 (XPNPEP1); SUBSTANCE-P; GENE; HYPERTENSION; BRADYKININ;

D O I：

10.1111/j.1872-034X.2011.00870.x

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Aim: To investigate XPNPEP1 rs17095355 polymorphism in biliary atresia (BA) patients and to determine whether there is an association between XPNPEP1 gene polymorphism and susceptibility to BA in a Thai population.

引用

页码：1249 / 1252

页数：4

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