Movement disorders in 2016: from genes to phenotypes

Paolo Calabresi, Nicola Tambasco

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

N/A
Original languageEnglish
Pages (from-to)9-10
Number of pages2
JournalLANCET NEUROLOGY
Volume16
DOIs
Publication statusPublished - 2017

Keywords

  • Genetic Variation
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Movement Disorders
  • Mutation
  • Phenotype

Fingerprint

Dive into the research topics of 'Movement disorders in 2016: from genes to phenotypes'. Together they form a unique fingerprint.

Cite this