Skip to search boxSkip to navigationSkip to main content

Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

  • the Global Parkinson’s Genetic Program (GP2)
    ,
  • Lara M. Lange(Author)
    ,
  • Micol Avenali(Author)
    ,
  • Melina Ellis(Author)
    ,
  • Anastasia Illarionova(Author)
    ,
  • Ignacio J. Keller Sarmiento(Author)
  • University of Lübeck
    ,
  • IRCCS Mondino Foundation
    ,
  • Università degli Studi di Cagliari
    ,
  • Concord Hospital
    ,
  • ANZAC Research Institute
    ,
  • Faculty of Medicine and Health
Research Output:
Contribution to journal
Comment/debate

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Comment/debate

Original language

English

Article number

133

Journal (Volume, Issue Number)

npj Parkinson's Disease (Volume 9, Issue 1)

Publication milestones

  • Published - 12/2023

Publication status

Published - 12/2023

Publication IDs

  • Scopus: 85171453011

Abstract

Correction to: npj Parkinson’s Disease, published online 27 June 2023 In this article the Global Parkinson’s Genetics Program (GP2) members names and affiliations were missing in the main author list of the Original article which are listed in the below.