Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?

the Global Parkinson's Genetics Program (GP2)

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
JournalMovement Disorders
DOIs
Publication statusAccepted/In press - 2024
Externally publishedYes

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

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