Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease
Author:
Funder
University of Lagos Central Research Committee
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference20 articles.
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2. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;A Zimprich;Neuron,2004
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4. []Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson’ disease: a case-control study;DG Healy;Lancet Neurol,2008
5. LRRK2 G2019S in the North African population: a review;HTS Benamer;Eur Neurol,2010
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1. The p.Gly2019Ser is the commonest pathogenic mutation in the LRRK2 gene among Egyptians with familial and sporadic Parkinson's disease;2024-07-01
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3. The Landscape of Monogenic Parkinson’s Disease in Populations of Non-European Ancestry: A Narrative Review;Genes;2023-11-17
4. Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study;The Lancet Neurology;2023-11
5. Transforming Parkinson's Care in Africa (TraPCAf): protocol for a multimethodology National Institute for Health and Care Research Global Health Research Group project;BMC Neurology;2023-10-19
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