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)

doi:10.1038/s41531-023-00560-7

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)

Producción científica: Contribución a una revista › Comentario/Debate

Resumen

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.

Idioma original	Inglés
Número de artículo	133
Publicación	npj Parkinson's Disease
Volumen	9
N.º	1
DOI	https://doi.org/10.1038/s41531-023-00560-7
Estado	Publicada - dic. 2023
Publicado de forma externa	Sí

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10.1038/s41531-023-00560-7

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

abstract = "Correction to: npj Parkinson{\textquoteright}s Disease, published online 27 June 2023 In this article the Global Parkinson{\textquoteright}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.",

author = "{the Global Parkinson{\textquoteright}s Genetic Program (GP2)} and Lange, {Lara M.} and Micol Avenali and Melina Ellis and Anastasia Illarionova and {Keller Sarmiento}, {Ignacio J.} and Tan, {Ai Huey} and Harutyun Madoev and Caterina Galandra and Johanna Junker and Karisha Roopnarain and Justin Solle and Claire Wegel and Fang, {Zih Hua} and Peter Heutink and Kumar, {Kishore R.} and Lim, {Shen Yang} and Valente, {Enza Maria} and Mike Nalls and Cornelis Blauwendraat and Andrew Singleton and Niccolo Mencacci and Katja Lohmann and Christine Klein and Gatto, {Emilia M.} and Marcelo Kauffman and Samson Khachatryan and Zaruhi Tavadyan and Shepherd, {Claire E.} and Julie Hunter and Renter{\'i}a, {Miguel E.} and Sulev Koks and Alexander Zimprich and Schumacher-Schuh, {Artur F.} and Carlos Rieder and Awad, {Paula Saffie} and Vitor Tumas and Sarah Camargos and Fon, {Edward A.} and Oury Monchi and Ted Fon and Galleguillos, {Benjamin Pizarro} and Marcelo Miranda and Bustamante, {Maria Leonor} and Patricio Olguin and Pedro Chana and Beisha Tang and Huifang Shang and Jifeng Guo and Piu Chan and Mario Cornejo-Olivas",

note = "Publisher Copyright: {\textcopyright} 2023, Springer Nature Limited.",

year = "2023",

month = dec,

doi = "10.1038/s41531-023-00560-7",

language = "Ingl{\'e}s",

volume = "9",

journal = "npj Parkinson's Disease",

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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).
En: npj Parkinson's Disease, Vol. 9, N.º 1, 133, 12.2023.

Producción científica: Contribución a una revista › Comentario/Debate

TY - JOUR

T1 - Author Correction

T2 - 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)

AU - the Global Parkinson’s Genetic Program (GP2)

AU - Lange, Lara M.

AU - Avenali, Micol

AU - Ellis, Melina

AU - Illarionova, Anastasia

AU - Keller Sarmiento, Ignacio J.

AU - Tan, Ai Huey

AU - Madoev, Harutyun

AU - Galandra, Caterina

AU - Junker, Johanna

AU - Roopnarain, Karisha

AU - Solle, Justin

AU - Wegel, Claire

AU - Fang, Zih Hua

AU - Heutink, Peter

AU - Kumar, Kishore R.

AU - Lim, Shen Yang

AU - Valente, Enza Maria

AU - Nalls, Mike

AU - Blauwendraat, Cornelis

AU - Singleton, Andrew

AU - Mencacci, Niccolo

AU - Lohmann, Katja

AU - Klein, Christine

AU - Gatto, Emilia M.

AU - Kauffman, Marcelo

AU - Khachatryan, Samson

AU - Tavadyan, Zaruhi

AU - Shepherd, Claire E.

AU - Hunter, Julie

AU - Rentería, Miguel E.

AU - Koks, Sulev

AU - Zimprich, Alexander

AU - Schumacher-Schuh, Artur F.

AU - Rieder, Carlos

AU - Awad, Paula Saffie

AU - Tumas, Vitor

AU - Camargos, Sarah

AU - Fon, Edward A.

AU - Monchi, Oury

AU - Fon, Ted

AU - Galleguillos, Benjamin Pizarro

AU - Miranda, Marcelo

AU - Bustamante, Maria Leonor

AU - Olguin, Patricio

AU - Chana, Pedro

AU - Tang, Beisha

AU - Shang, Huifang

AU - Guo, Jifeng

AU - Chan, Piu

AU - Cornejo-Olivas, Mario

PY - 2023/12

Y1 - 2023/12

N2 - 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.

AB - 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.

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U2 - 10.1038/s41531-023-00560-7

DO - 10.1038/s41531-023-00560-7

M3 - Comentario/Debate

AN - SCOPUS:85171453011

SN - 2373-8057

VL - 9

JO - npj Parkinson's Disease

JF - npj Parkinson's Disease

IS - 1

M1 - 133

ER -