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AARS, ARG329HIS

 
National Institutes of Health

Related topics

Related topics

1 relation
Charcot-Marie-Tooth Disease, Axonal, Type 2n

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defect.
Mutations in genes encoding aminoacyl-tRNA synthetases are known to cause leukodystrophies and genetic leukoencephalopathies… Expand
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2011
2011
Uvođenje mutacija u sintetsko mjesto izoleucil-tRNA-sintetaze s ciljem rasvjetljavanja mehanizama hidrolitičkog popravka
Aminoacil-tRNA-sintetaze (aaRS) su enzimi koji kataliziraju reakciju kovalentnog vezanja aminokiseline na odgovarajucu molekulu… Expand
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Highly Cited
2011
Highly Cited
2011
An evolved aminoacyl-tRNA synthetase with atypical polysubstrate specificity.
We have employed a rapid fluorescence-based screen to assess the polyspecificity of several aminoacyl-tRNA synthetases (aaRSs… Expand
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