MRPS22 gene

Known as: GK002, C3orf5, CHROMOSOME 3 OPEN READING FRAME 5 
 

Topic mentions per year

Topic mentions per year

2004-2017
02420042017

Papers overview

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2017
2017
MRPS22 gene defect is a very rare newly discovered mitochondrial disorder. We report a 4-month-old severely affected male infant… (More)
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2017
2017
In the original publication of the article, the title was incorrectly written as “The cerebellum is a common site of affection in… (More)
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2017
2017
Letter to the Editor. We read with interest the article by Kilic et al. about a 4 months old male with dysmorphism, hypotonia… (More)
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2017
2017
The genetic basis of earlobe attachment has been a matter of debate since the early 20th century, such that geneticists argue… (More)
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2014
2014
The five complexes of the mitochondrial respiratory chain (MRC) supply most organs and tissues with ATP produced by oxidative… (More)
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2012
2012
Here, we present new genetic and morphological evidence that human tumors consist of two distinct metabolic compartments. First… (More)
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2012
2012
CONTEXT Hypertension, typically considered a disorder of adulthood, is now emerging in adolescence. This is mainly due to the… (More)
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2011
2011
The oxidative phosphorylation (OXPHOS) system is under control of both the mitochondrial and the nuclear genomes; 13 subunits are… (More)
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2008
2008
Mutations in mitochondrial small subunit ribosomal proteins MRPS16 or MRPS22 cause severe, fatal respiratory chain dysfunction… (More)
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2004
2004
A translocation breakpoint 171 kb 5' of the transcription start of FOXL2 causes blepharophimosis/ptosis/epicanthus inversus… (More)
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