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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Detalles Bibliográficos
Autores principales: Pagliaroli, Luca, Vereczkei, Andrea, Padmanabhuni, Shanmukha Sampath, Tarnok, Zsanett, Farkas, Luca, Nagy, Peter, Rizzo, Renata, Wolanczyk, Tomasz, Szymanska, Urszula, Kapisyzi, Mira, Basha, Entela, Koumoula, Anastasia, Androutsos, Christos, Tsironi, Vaia, Karagiannidis, Iordanis, Paschou, Peristera, Barta, Csaba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457023/
https://www.ncbi.nlm.nih.gov/pubmed/32922348
http://dx.doi.org/10.3389/fneur.2020.00803

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457023/
https://www.ncbi.nlm.nih.gov/pubmed/32922348
http://dx.doi.org/10.3389/fneur.2020.00803

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