LRRK2 Mutations and Asian Disease-Associated Variants in the First Parkinson's Disease Cohort from Kazakhstan

BACKGROUND: LRRK2 mutations have emerged as the most prevalent and potentially treatable determinants of Parkinson's disease (PD). Peculiar geographic distribution of these mutations has triggered an interest in genotyping PD cohorts of different ethnic backgrounds for LRRK. OBJECTIVE: Here, we...

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Detalles Bibliográficos
Autores principales: Kaiyrzhanov, Rauan, Aitkulova, Akbota, Shashkin, Chingiz, Zharkinbekova, Nazira, Rizig, Mie, Zholdybayeva, Elena, Jarmukhanov, Zharkyn, Akhmetzhanov, Vadim, Kaishibayeva, Gulnaz, Khaibullin, Talgat, Karimova, Altynay, Akshulakov, Serik, Bralov, Askhat, Kissamedenov, Nurlan, Seidinova, Zhanar, Taskinbayeva, Anjela, Muratbaikyzy, Aliya, Houlden, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049866/
https://www.ncbi.nlm.nih.gov/pubmed/32148752
http://dx.doi.org/10.1155/2020/2763838

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049866/
https://www.ncbi.nlm.nih.gov/pubmed/32148752
http://dx.doi.org/10.1155/2020/2763838

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