A copy number variation in human NCF1 and its pseudogenes
about
Genetic disorders coupled to ROS deficiencyDiabetes, renal and cardiovascular disease in p47 phox-/- chronic granulomatous disease.Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion.Copy number variations of the ATP-binding cassette transporter ABCC6 gene and its pseudogenes.Functional pseudogenes inhibit the superoxide production.A response to: BAK1 gene variation and abdominal aortic aneurysms—results may have been prematurely overrated. Questions of sequence fidelity, intraorganismal genetic heterogeneity, the nature of pseudogenes, and RNA editing.
P2860
A copy number variation in human NCF1 and its pseudogenes
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
name
A copy number variation in human NCF1 and its pseudogenes
@ast
A copy number variation in human NCF1 and its pseudogenes
@en
A copy number variation in human NCF1 and its pseudogenes.
@nl
type
label
A copy number variation in human NCF1 and its pseudogenes
@ast
A copy number variation in human NCF1 and its pseudogenes
@en
A copy number variation in human NCF1 and its pseudogenes.
@nl
prefLabel
A copy number variation in human NCF1 and its pseudogenes
@ast
A copy number variation in human NCF1 and its pseudogenes
@en
A copy number variation in human NCF1 and its pseudogenes.
@nl
P2093
P2860
P356
P1433
P1476
A copy number variation in human NCF1 and its pseudogenes
@en
P2093
Isfahan Chambers
Qingwei Wang
Tiffany Brunson
P2860
P2888
P356
10.1186/1471-2156-11-13
P577
2010-02-23T00:00:00Z
P5875
P6179
1052539923