Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype"

Neuromuscul Disord. 2020 Mar;30(3):265-266. doi: 10.1016/j.nmd.2020.01.003. Epub 2020 Jan 30.
No abstract available

Keywords: ARAN-NM; HINT1; Neurodevelopmental; Psychiatric.

Publication types

  • Letter
  • Comment

MeSH terms

  • Humans
  • Isaacs Syndrome*
  • Mental Disorders*
  • Mutation
  • Nerve Tissue Proteins / genetics
  • Phenotype

Substances

  • HINT1 protein, human
  • Nerve Tissue Proteins