Genetic risk factors and role of immune dysfunction in FTLD

Research output: Contribution to journalArticlepeer-review


A new study has identified novel genes involved in sporadic frontotemporal lobar degeneration with neuronal inclusions of TAR DNA-binding protein 43. These findings might enable the elucidation of pathogenic mechanisms of the disease and have implications for the identification of potential therapeutic targets.

Original languageEnglish
Pages (from-to)250-251
JournalNature Reviews Neurology
Issue number5
Publication statusPublished - Jan 1 2019

ASJC Scopus subject areas

  • Clinical Neurology
  • Cellular and Molecular Neuroscience


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