Exome-Wide Analyses in Paroxysmal Kinesigenic Dyskinesia Confirm TMEM151A as a Novel Causative Gene

Mov Disord. 2022 Mar;37(3):641-643. doi: 10.1002/mds.28904. Epub 2021 Dec 31.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chorea* / genetics
  • Dystonia* / genetics
  • Exome
  • Humans

Supplementary concepts

  • Familial paroxysmal dystonia