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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499986/ https://www.ncbi.nlm.nih.gov/pubmed/37704671 http://dx.doi.org/10.1038/s41531-023-00560-7 |
| _version_ | 1785105828567580672 |
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| author | Lange, Lara M. Avenali, Micol Ellis, Melina Illarionova, Anastasia Keller Sarmiento, Ignacio J. Tan, Ai-Huey Madoev, Harutyun Galandra, Caterina Junker, Johanna Roopnarain, Karisha Solle, Justin Wegel, Claire Fang, Zih-Hua Heutink, Peter Kumar, Kishore R. Lim, Shen-Yang Valente, Enza Maria Nalls, Mike Blauwendraat, Cornelis Singleton, Andrew Mencacci, Niccolo Lohmann, Katja Klein, Christine |
| author_facet | Lange, Lara M. Avenali, Micol Ellis, Melina Illarionova, Anastasia Keller Sarmiento, Ignacio J. Tan, Ai-Huey Madoev, Harutyun Galandra, Caterina Junker, Johanna Roopnarain, Karisha Solle, Justin Wegel, Claire Fang, Zih-Hua Heutink, Peter Kumar, Kishore R. Lim, Shen-Yang Valente, Enza Maria Nalls, Mike Blauwendraat, Cornelis Singleton, Andrew Mencacci, Niccolo Lohmann, Katja Klein, Christine |
| author_sort | Lange, Lara M. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10499986 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Nature Publishing Group UK |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-104999862023-09-15 Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) Lange, Lara M. Avenali, Micol Ellis, Melina Illarionova, Anastasia Keller Sarmiento, Ignacio J. Tan, Ai-Huey Madoev, Harutyun Galandra, Caterina Junker, Johanna Roopnarain, Karisha Solle, Justin Wegel, Claire Fang, Zih-Hua Heutink, Peter Kumar, Kishore R. Lim, Shen-Yang Valente, Enza Maria Nalls, Mike Blauwendraat, Cornelis Singleton, Andrew Mencacci, Niccolo Lohmann, Katja Klein, Christine NPJ Parkinsons Dis Author Correction Nature Publishing Group UK 2023-09-13 /pmc/articles/PMC10499986/ /pubmed/37704671 http://dx.doi.org/10.1038/s41531-023-00560-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
| spellingShingle | Author Correction Lange, Lara M. Avenali, Micol Ellis, Melina Illarionova, Anastasia Keller Sarmiento, Ignacio J. Tan, Ai-Huey Madoev, Harutyun Galandra, Caterina Junker, Johanna Roopnarain, Karisha Solle, Justin Wegel, Claire Fang, Zih-Hua Heutink, Peter Kumar, Kishore R. Lim, Shen-Yang Valente, Enza Maria Nalls, Mike Blauwendraat, Cornelis Singleton, Andrew Mencacci, Niccolo Lohmann, Katja Klein, Christine Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| title | Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| title_full | Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| title_fullStr | Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| title_full_unstemmed | Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| title_short | Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| title_sort | author correction: elucidating causative gene variants in hereditary parkinson’s disease in the global parkinson’s genetics program (gp2) |
| topic | Author Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499986/ https://www.ncbi.nlm.nih.gov/pubmed/37704671 http://dx.doi.org/10.1038/s41531-023-00560-7 |
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