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

Gaia Scarpini, Carlotta Spagnoli, Grazia Gabriella Salerno, Susanna Rizzi, Daniele Frattini, Carlo Fusco

Research output: Contribution to journalLetter

Original languageEnglish
Number of pages1
JournalNeuromuscular Disorders
Volume29
Issue number12
DOIs
Publication statusPublished - Dec 2019

Keywords

  • HINT1
  • Mood disorder
  • Neuromyotonia
  • Neuropathy

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Neurology
  • Clinical Neurology
  • Genetics(clinical)

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