A case of myelopathy, myopathy, peripheral neuropathy and subcortical grey matter degeneration associated with recessive compound heterozygous POLG1 mutations Journal Articles Refereed uri icon

Overview

Published in

  • Neuromuscular Disorders

Time

Date/time value

  • 2012

Identity

Digital Object Identifier (DOI)

  • 10.1016/j.nmd.2011.10.017

Additional Document Info

Parent Title

  • Neuromuscular Disorders

Volume

  • 22

Issue

  • 5

Publisher

  • Pergamon