Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome

Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome

Background: Tourette Syndrome (TS) is a neurodevelopmental disorder that presents with motor and vocal tics early in childhood. The aim of this study was to investigate genetic variants in the 3' untranslated region (3'UTR) of TS candidate genes with a putative link to microRNA (miRNA) med...

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Main Authors: Luca Pagliaroli, Andrea Vereczkei, Shanmukha Sampath Padmanabhuni, Zsanett Tarnok, Luca Farkas, Peter Nagy, Renata Rizzo, Tomasz Wolanczyk, Urszula Szymanska, Mira Kapisyzi, Entela Basha, Anastasia Koumoula, Christos Androutsos, Vaia Tsironi, Iordanis Karagiannidis, Peristera Paschou, Csaba Barta
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-08-01
Series:Frontiers in Neurology
Subjects:
3'UTR
genetic variation
microRNA
SNP
Tourette Syndrome
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2020.00803/full

Internet

https://www.frontiersin.org/article/10.3389/fneur.2020.00803/full

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