GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease.

Détails

ID Serval
serval:BIB_DFB754DDDD7C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease.
Périodique
European Journal of Neurology
Auteur⸱e⸱s
Jasinska-Myga B., Wider C., Opala G., Krygowska-Wajs A., Barcikowska M., Czyzewski K., Baker M., Rademakers R., Uitti R.J., Farrer M.J., Ross O.A., Wszolek Z.K.
ISSN
1468-1331[electronic], 1351-5101[linking]
Statut éditorial
Publié
Date de publication
2009
Volume
16
Numéro
8
Pages
909-911
Langue
anglais
Résumé
BACKGROUND AND PURPOSE: A single nucleotide polymorphism in the 3'-untranslated region of the progranulin gene (GRN; 3'UTR+78C>T; rs5848) was reported to alter the risk for frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U). rs5848 is located within a micro-RNA binding site and affects the expression of GRN.
METHODS: As FTLD-U patients often present with parkinsonism, we investigated the association of GRN rs5848 and risk of Parkinson's disease in two Caucasian patient-control series (n = 1413) from the US and Poland.
RESULTS: No association was observed between rs5848 and susceptibility to Parkinson's disease (individual series and combined analysis).
CONCLUSIONS: This finding shows that GRN rs5848 does not affect the risk of Parkinson's disease in the US and Polish populations.
Mots-clé
Adult, Aged, Aged, 80 and over, European Continental Ancestry Group/genetics, Female, Gene Frequency, Genetic Predisposition to Disease, Genotype, Humans, Intercellular Signaling Peptides and Proteins/genetics, Male, Middle Aged, Parkinson Disease/epidemiology, Parkinson Disease/genetics, Poland/epidemiology, Polymorphism, Single Nucleotide, Risk Factors, United States/epidemiology, Young Adult
Pubmed
Création de la notice
24/09/2010 19:03
Dernière modification de la notice
20/08/2019 17:04
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