Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)

Lange, Lara; Avenali, Micol; Ellis, Melina; Illarionova, Anastasia J.; Sarmiento, Ignacio Keller; Tan, Ai-Huey; Madoev, Harutyun; Galandra, Caterina; Junker, Johanna; Roopnarain, Karisha; Solle, Justin; Wegel, Claire; Fang, Zih-Hua; Heutink, Peter R.; Kumar, Kishore; Lim, Shen-Yang; Valente, Enza Maria; Nalls, Mike; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolo; Lohmann, Katja; Klein, Christine

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dc.contributor.author	Illarionova, Anastasia
dc.contributor.author	Fang, Zih-Hua
dc.contributor.author	Heutink, Peter
dc.date.accessioned	2024-02-07T15:19:06Z
dc.date.available	2024-02-07T15:19:06Z
dc.date.issued	2023
dc.identifier.issn	2373-8057
dc.identifier.uri	http://hdl.handle.net/10900/150869
dc.language.iso	en	en
dc.publisher	Berlin : Nature Portfolio	de_DE
dc.relation.uri	http://dx.doi.org/10.1038/s41531-023-00526-9
dc.subject.ddc	610	de_DE
dc.subject.ddc	570	de_DE
dc.title	Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)	de_DE
dc.type	Article	de_DE
utue.quellen.id	20230928000000_00735
utue.personen.roh	Lange, Lara
utue.personen.roh	Avenali, Micol
utue.personen.roh	Ellis, Melina
utue.personen.roh	Illarionova, Anastasia J.
utue.personen.roh	Sarmiento, Ignacio Keller
utue.personen.roh	Tan, Ai-Huey
utue.personen.roh	Madoev, Harutyun
utue.personen.roh	Galandra, Caterina
utue.personen.roh	Junker, Johanna
utue.personen.roh	Roopnarain, Karisha
utue.personen.roh	Solle, Justin
utue.personen.roh	Wegel, Claire
utue.personen.roh	Fang, Zih-Hua
utue.personen.roh	Heutink, Peter R.
utue.personen.roh	Kumar, Kishore
utue.personen.roh	Lim, Shen-Yang
utue.personen.roh	Valente, Enza Maria
utue.personen.roh	Nalls, Mike
utue.personen.roh	Blauwendraat, Cornelis
utue.personen.roh	Singleton, Andrew
utue.personen.roh	Mencacci, Niccolo
utue.personen.roh	Lohmann, Katja
utue.personen.roh	Klein, Christine
dcterms.isPartOf.ZSTitelID	Npj Parkinsons Disease	de_DE
dcterms.isPartOf.ZS-Issue	1	de_DE
dcterms.isPartOf.ZS-Volume	9	de_DE
utue.fakultaet	Sonstige