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

Salvatore Rossi, Gabriella Silvestri, Alessia Perna, Anna Modoni, Enrico Silvio Bertini, Vittorio Riso, Tommaso Filippo Nicoletti

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

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Original languageEnglish
Pages (from-to)N/A-N/A
JournalNeuromuscular Disorders
DOIs
Publication statusPublished - 2020

Keywords

  • ARAN-NM
  • HINT1
  • Neurodevelopmental
  • Psychiatric

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