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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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Neurology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7457023/
https://ncbi.nlm.nih.gov/pubmed/32922348
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.00803
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