Whole-Exome Sequencing Identified Rare Variants in PCDHGB1 in Patients with Adult-Onset Dystonia

Mov Disord. 2022 May;37(5):1099-1101. doi: 10.1002/mds.28965. Epub 2022 Mar 1.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Dystonic Disorders* / genetics
  • Exome
  • Exome Sequencing
  • Humans