Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) ; volume:9 ; number:1 ; day:12 ; month:9 ; year:2023 ; pages:1-6 ; date:12.2023
npj Parkinson's Disease ; 9, Heft 1 (12.9.2023), 1-6, 12.2023
- Urheber
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Towns, Clodagh
Richer, Madeleine
Jasaityte, Simona
Stafford, Eleanor J.
Joubert, Julie
Antar, Tarek
Martinez-Carrasco, Alejandro
Makarious, Mary B.
Casey, Bradford
Vitale, Dan
Levine, Kristin
Leonard, Hampton
Pantazis, Caroline B.
Screven, Laurel A.
Hernandez, Dena G.
Wegel, Claire E.
Solle, Justin
Nalls, Mike A.
Blauwendraat, Cornelis
Singleton, Andrew B.
Tan, Manuela M. X.
Iwaki, Hirotaka
Morris, Huw R.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41531-023-00533-w
- URN
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urn:nbn:de:101:1-2024020515101745997498
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:36 MESZ
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Beteiligte
- Towns, Clodagh
- Richer, Madeleine
- Jasaityte, Simona
- Stafford, Eleanor J.
- Joubert, Julie
- Antar, Tarek
- Martinez-Carrasco, Alejandro
- Makarious, Mary B.
- Casey, Bradford
- Vitale, Dan
- Levine, Kristin
- Leonard, Hampton
- Pantazis, Caroline B.
- Screven, Laurel A.
- Hernandez, Dena G.
- Wegel, Claire E.
- Solle, Justin
- Nalls, Mike A.
- Blauwendraat, Cornelis
- Singleton, Andrew B.
- Tan, Manuela M. X.
- Iwaki, Hirotaka
- Morris, Huw R.
- SpringerLink (Online service)
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