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LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact
| Autores principales: | , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley & Sons, Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248088/ https://www.ncbi.nlm.nih.gov/pubmed/33433017 http://dx.doi.org/10.1002/mds.28452 |
| _version_ | 1783716652151472128 |
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| author | Beetz, Christian Westenberger, Ana Al‐Ali, Ruslan Ameziane, Najim Alhashmi, Nadia Boustany, Rose‐Mary Al Mutairi, Fuad Alfadhel, Majid Al‐Hassnan, Zuhair AlSayed, Moenaldeen Kandaswamy, Krishna K. Paknia, Omid Skrahina, Volha Rolfs, Arndt Bauer, Peter |
| author_facet | Beetz, Christian Westenberger, Ana Al‐Ali, Ruslan Ameziane, Najim Alhashmi, Nadia Boustany, Rose‐Mary Al Mutairi, Fuad Alfadhel, Majid Al‐Hassnan, Zuhair AlSayed, Moenaldeen Kandaswamy, Krishna K. Paknia, Omid Skrahina, Volha Rolfs, Arndt Bauer, Peter |
| author_sort | Beetz, Christian |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-8248088 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | John Wiley & Sons, Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-82480882021-07-02 LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact Beetz, Christian Westenberger, Ana Al‐Ali, Ruslan Ameziane, Najim Alhashmi, Nadia Boustany, Rose‐Mary Al Mutairi, Fuad Alfadhel, Majid Al‐Hassnan, Zuhair AlSayed, Moenaldeen Kandaswamy, Krishna K. Paknia, Omid Skrahina, Volha Rolfs, Arndt Bauer, Peter Mov Disord Regular Issue Articles John Wiley & Sons, Inc. 2021-01-12 2021-04 /pmc/articles/PMC8248088/ /pubmed/33433017 http://dx.doi.org/10.1002/mds.28452 Text en © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Regular Issue Articles Beetz, Christian Westenberger, Ana Al‐Ali, Ruslan Ameziane, Najim Alhashmi, Nadia Boustany, Rose‐Mary Al Mutairi, Fuad Alfadhel, Majid Al‐Hassnan, Zuhair AlSayed, Moenaldeen Kandaswamy, Krishna K. Paknia, Omid Skrahina, Volha Rolfs, Arndt Bauer, Peter LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact |
| title |
LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact |
| title_full |
LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact |
| title_fullStr |
LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact |
| title_full_unstemmed |
LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact |
| title_short |
LRRK2 Loss‐of‐Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact |
| title_sort | lrrk2 loss‐of‐function variants in patients with rare diseases: no evidence for a phenotypic impact |
| topic | Regular Issue Articles |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248088/ https://www.ncbi.nlm.nih.gov/pubmed/33433017 http://dx.doi.org/10.1002/mds.28452 |
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