Association between p47phox pseudogenes and inflammatory bowel disease

被引：9

作者：

Harbord, M ^{[1
]}

Hankin, A ^{[1
]}

Bloom, S ^{[1
]}

Mitchison, H ^{[1
]}

机构：

[1] UCL, Rayne Inst, Dept Med, London WC1E 6JJ, England

来源：

BLOOD | 2003年 / 101卷 / 08期

关键词：

D O I：

10.1182/blood-2002-10-3060

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：3337 / 3337

页数：1

共 10 条

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[5] Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion:: significance for A47° chronic granulomatous disease carrier detection
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[7] Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease
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[8] Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
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[J]. NATURE GENETICS, 1996, 14 (02) : 199 - 202
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