A CASE OF NEUROMYOTONIA AND AXONAL MOTOR NEUROPATHY: A REPORT OF A HINT1 MUTATION IN THE UNITED STATES Article

cited authors

  • Jerath, Nivedita U.; Shy, Michael E.; Grider, Tiffany; Gutmann, Ludwig

authors

Publication Date

  • December 1, 2015

webpage

published in

category

keywords

  • EMG
  • HINT1
  • hereditary neuropathy
  • mutation
  • neurogenetics
  • neuromyotonia

start page

  • 1110

end page

  • 1113

volume

  • 52

issue

  • 6