KIAA2022 gene

Known as: KIAA2022, MRX98, XPN 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2017
02419762017

Papers overview

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2016
2016
BACKGROUND Mutations in the KIAA2022 gene have been reported in male patients with X-linked intellectual disability, and related… (More)
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2015
2015
To the Editor: X-linked intellectual disability (XLID) accounts for ∼10% of intellectually disabled males, and much attention has… (More)
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2013
2013
Existence of a discrete new X-linked intellectual disability (XLID) syndrome due to KIAA2022 deficiency was questioned by… (More)
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2013
2013
X-linked mental retardation (XLMR) is a common cause of moderate to severe intellectual disability in males. XLMR protein related… (More)
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2011
2011
Simultaneous measurement of gene expression on a genomic scale can be accomplished using microarray technology or by sequencing… (More)
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2007
2007
BACKGROUND Xanthogranulomatous pyelonephritis (XPN), a rare form ofchronicpyelonephritis, is commonly associated with lithiasis… (More)
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2004
2004
BACKGROUND Mental retardation (MR) affects 2-3% of the human population and some of these cases are genetically determined… (More)
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2002
2002
Xanthogranulomatous pyelonephritis (XPN) is the result of chronic renal infection. It is very rare in childhood and the focal… (More)
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1990
1990
A case of multifocal xanthogranulomatous pyelonephritis (XPN) in childhood diagnosed by ultrasound, computed tomography and… (More)
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1983
1983
Analysis of 87 cases of xanthogranulomatous pyelonephritis ( XPN ) from 1958 to 1983 (14 males, 73 females, ages 13-85) revealed… (More)
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