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Lack of Association of the rs11655081 ARSG Gene with Blepharospasm

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Autore
Siokas V., Kardaras D., Aloizou A.-M., Asproudis I., Boboridis K.G., Papageorgiou E., Spandidos D.A., Tsatsakis A., Tsironi E.E., Dardiotis E.
Data
2019
Language
en
DOI
10.1007/s12031-018-1255-3
Soggetto
arylsulfatase
arylsulfatase g
unclassified drug
arylsulfatase
arylsulfatase G, human
adult
aged
Article
blepharospasm
blood sampling
cohort analysis
controlled study
female
gene frequency
genetic association
genetic risk
genetic variability
genotype
Greece
human
inheritance
major clinical study
male
middle aged
risk assessment
single nucleotide polymorphism
blepharospasm
genetics
Arylsulfatases
Blepharospasm
Humans
Polymorphism, Single Nucleotide
Springer New York LLC
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Abstract
Blepharospasm (BSP) is a sub-phenotype of focal dystonia. A few genetic risk factors are considered to be implicated in the risk of developing BSP. There is recent evidence, based on results from GWAS and meta-analyses, to suggest that arylsulfatase G (ARSG), and more specifically rs11655081, is implicated in focal dystonia. The aim of the present study was to evaluate the effect of rs11655081 ARSG on BSP. A Greek cohort, which consisted of 206 BSP patients and an equal number of healthy controls, was genotyped for rs11655081. Only a marginal trend for the association between rs11655081 and the risk of BSP was found in the over-dominant model of inheritance [odds ratio, OR (95% confidence interval, CI): 0.64 (0.38–1.07), p = 0.088]. It is rather unlikely that rs11655081 across ARSG is a major genetic risk contributor for BSP. © 2019, Springer Science+Business Media, LLC, part of Springer Nature.
URI
http://hdl.handle.net/11615/79037
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19743]
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