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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

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Highly Cited
2015
Highly Cited
2015
Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defect.
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… 
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