DNMT1-complex disorder caused by a novel mutation associated with an overlapping phenotype of autosomal-dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) and hereditary sensory neuropathy with dementia and hearing loss (HSN1E)

Alessia Catania, Lorenzo Peverelli, Silvia Tabano, Daniele Ghezzi, Costanza Lamperti

Research output: Contribution to journalLetter

Original languageEnglish
Pages (from-to)1963-1966
JournalNeurological Sciences
Volume40
Issue number9
DOIs
Publication statusPublished - Jan 1 2019

ASJC Scopus subject areas

  • Dermatology
  • Clinical Neurology
  • Psychiatry and Mental health

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