A meta-analysis of the prevalence of the mutation LRRK2 G2019S in patients with Parkinson's disease in Africa
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference33 articles.
1. Parkinson’s disease in Saudi patients: a genetic study;Al-Mubarak;PLoS One,2015
2. Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson’s disease patients;Bardien;Mov. Disord.,2013
3. Evidence for prehistoric origins of the G2019S mutation in the North African Berber population;Ben El Haj;PLoS One,2017
4. LRRK2 G2019S mutation: prevalence and clinical features in moroccans with Parkinson's disease;Bouhouche;Parkinson's Disease,2017
5. Screening LRRK2 gene mutations in patients with Parkinson’s disease in Ghana;Cilia;J. Neurol.,2012
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1. Role of Caffeine in the Age-related Neurodegenerative Diseases: A Review;Mini-Reviews in Medicinal Chemistry;2022-11
2. Parkinson's disease: The prevalence of the LRRK2-G2019S mutation among the population of the South-West of Morocco;Gene Reports;2022-06
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