Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy
Neurology, 06/08/2012
Zhao Z et al. – An AARS mutation caused dHMN in a Chinese family. Alanyl–tRNA synthetase (AARS) mutations result in not only a Charcot–Marie–Tooth disease (CMT) phenotype but also a dHMN phenotype.



