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NARS2 gene

Known as: SLM5, ASPARAGINYL-tRNA SYNTHETASE 2, ASPARAGINYL-tRNA SYNTHETASE, MITOCHONDRIAL 
National Institutes of Health

Papers overview

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2020
2020
Autozygosity-driven exome analysis has been shown effective for identification of genes underlying recessive diseases especially… Expand
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2018
2018
BACKGROUND Infantile epileptic encephalopathy is a heterogeneous condition that has been associated with variants in more than… Expand
2017
2017
Here we present four unrelated families with six individuals that have infantile-onset developmental delay/regression and… Expand
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Highly Cited
2015
Highly Cited
2015
Alpers syndrome is a progressive neurodegenerative disorder that presents in infancy or early childhood and is characterized by… Expand
2015
2015
Here we demonstrate association of variants in the mitochondrial asparaginyl-tRNA synthetase NARS2 with human hearing loss and… Expand
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2015
2015
A homozygous missense mutation (c.822G>C) was found in the gene encoding the mitochondrial asparaginyl–tRNA synthetase (NARS2) in… Expand
2015
2015
Here we demonstrate association of variants in the mitochondrial asparaginyl-tRNA synthetase NARS2 with human hearing loss and… Expand
2014
2014
We report a pathogenic mutation in NARS2, a gene coding for an asparaginyl tRNA synthetase, previously not associated with a… Expand
Highly Cited
2008
Highly Cited
2008
Seed morphogenesis consists of embryogenesis and the development of maternal tissues such as the inner and outer integuments… Expand
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Highly Cited
1994
Highly Cited
1994
The MADS box motif is common to genes that regulate the pattern of flower development. To determine whether MADS box genes also… Expand
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