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Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients
BACKGROUND: Fibroblast growth factor 20 (FGF20) is a neurotrophic factor preferentially expressed in the substantia nigra of rat brain and could be involved in dopaminergic neurons survival. Recently, a strong genetic association has been found between FGF20 gene and the risk of suffering from Parki...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183215/ https://www.ncbi.nlm.nih.gov/pubmed/15967032 http://dx.doi.org/10.1186/1471-2377-5-11 |
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author | Clarimon, Jordi Xiromerisiou, Georgia Eerola, Johanna Gourbali, Vanesa Hellström, Olli Dardiotis, Euthimios Peuralinna, Terhi Papadimitriou, Alexandros Hadjigeorgiou, George M Tienari, Pentti J Singleton, Andrew B |
author_facet | Clarimon, Jordi Xiromerisiou, Georgia Eerola, Johanna Gourbali, Vanesa Hellström, Olli Dardiotis, Euthimios Peuralinna, Terhi Papadimitriou, Alexandros Hadjigeorgiou, George M Tienari, Pentti J Singleton, Andrew B |
author_sort | Clarimon, Jordi |
collection | PubMed |
description | BACKGROUND: Fibroblast growth factor 20 (FGF20) is a neurotrophic factor preferentially expressed in the substantia nigra of rat brain and could be involved in dopaminergic neurons survival. Recently, a strong genetic association has been found between FGF20 gene and the risk of suffering from Parkinson's disease (PD). Our aim was to replicate this association in two independent populations. METHODS: Allelic, genotypic, and haplotype frequencies of four biallelic polymorphisms were assessed in 151 sporadic PD cases and 186 controls from Greece, and 144 sporadic PD patients and 135 controls from Finland. RESULTS: No association was found in any of the populations studied. CONCLUSION: Taken together, these findings suggest that common genetic variants in FGF20 are not a risk factor for PD in, at least, some European populations. |
format | Text |
id | pubmed-1183215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11832152005-08-06 Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients Clarimon, Jordi Xiromerisiou, Georgia Eerola, Johanna Gourbali, Vanesa Hellström, Olli Dardiotis, Euthimios Peuralinna, Terhi Papadimitriou, Alexandros Hadjigeorgiou, George M Tienari, Pentti J Singleton, Andrew B BMC Neurol Research Article BACKGROUND: Fibroblast growth factor 20 (FGF20) is a neurotrophic factor preferentially expressed in the substantia nigra of rat brain and could be involved in dopaminergic neurons survival. Recently, a strong genetic association has been found between FGF20 gene and the risk of suffering from Parkinson's disease (PD). Our aim was to replicate this association in two independent populations. METHODS: Allelic, genotypic, and haplotype frequencies of four biallelic polymorphisms were assessed in 151 sporadic PD cases and 186 controls from Greece, and 144 sporadic PD patients and 135 controls from Finland. RESULTS: No association was found in any of the populations studied. CONCLUSION: Taken together, these findings suggest that common genetic variants in FGF20 are not a risk factor for PD in, at least, some European populations. BioMed Central 2005-06-20 /pmc/articles/PMC1183215/ /pubmed/15967032 http://dx.doi.org/10.1186/1471-2377-5-11 Text en Copyright © 2005 Clarimon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Clarimon, Jordi Xiromerisiou, Georgia Eerola, Johanna Gourbali, Vanesa Hellström, Olli Dardiotis, Euthimios Peuralinna, Terhi Papadimitriou, Alexandros Hadjigeorgiou, George M Tienari, Pentti J Singleton, Andrew B Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients |
title | Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients |
title_full | Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients |
title_fullStr | Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients |
title_full_unstemmed | Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients |
title_short | Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients |
title_sort | lack of evidence for a genetic association between fgf20 and parkinson's disease in finnish and greek patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183215/ https://www.ncbi.nlm.nih.gov/pubmed/15967032 http://dx.doi.org/10.1186/1471-2377-5-11 |
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