Abstract
Several genetic variations have been associated with Parkinson disease in different populations over the past few years. Although a considerable number of worldwide populations have been screened for these variants, results from Sub-Saharan populations are very scarce in the literature. In the present report we have screened a cohort of Parkinson disease patients (n = 57) and healthy controls (n = 51) from Nigeria for mutations in the genes PRKN, LRRK2 and ATXN3. No pathogenic mutations were found in any of the genes. Hence, common pathogenic mutations in these genes, observed in several different populations, are not a frequent cause of Parkinson disease in Nigeria.
MeSH Terms
Adult
Aged
Ataxin-3
Case-Control Studies
Cohort Studies
DNA Mutational Analysis
Female
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Male
Middle Aged
Mutation
Nerve Tissue Proteins/genetics
Nigeria
Nuclear Proteins/genetics
Parkinson Disease/epidemiology,genetics
Protein Serine-Threonine Kinases/genetics
Repressor Proteins/genetics
Ubiquitin-Protein Ligases/genetics
Chemicals
Nerve Tissue Proteins
Nuclear Proteins
Repressor Proteins
Ubiquitin-Protein Ligases
parkin protein
LRRK2 protein, human
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Protein Serine-Threonine Kinases
ATXN3 protein, human
Ataxin-3
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Okubadejo Njideka
Neurology Unit, Department of Medicine, College of Medicine, University of Lagos, Lagos, Nigeria.
Britton Angela
Crews Cynthia
Akinyemi Rufus
Hardy John
Singleton Andrew
Bras Jose
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