Absence of the LRRK2 mutation in Emirati Parkinson’s disease patients in contrast to other Arab populations
BackgroundThe role of genetic factors in the pathogenesis of Parkinson’s disease (PD) is characterized by heterogeneity in specific genetic variations and their prevalence across different populations and geographic locations.ObjectiveTo investigate the frequency of the Leucine-rich repeat kinase 2...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2025-11-01
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| Col·lecció: | Frontiers in Aging Neuroscience |
| Matèries: | |
| Accés en línia: | https://www.frontiersin.org/articles/10.3389/fnagi.2025.1676115/full |
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