Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome

BACKGROUND: Genes involved in Tourette syndrome (TS) remain largely unknown. We aimed to identify genetic factors contributing to TS in a French cohort of 120 individuals using a combination of hypothesis-driven and exome-sequencing approaches. METHODS: We first sequenced exons of SLITRK1-6 and HDC...

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Detalles Bibliográficos
Autores principales: Depienne, Christel, Ciura, Sorana, Trouillard, Oriane, Bouteiller, Delphine, Leitão, Elsa, Nava, Caroline, Keren, Boris, Marie, Yannick, Guegan, Justine, Forlani, Sylvie, Brice, Alexis, Anheim, Mathieu, Agid, Yves, Krack, Paul, Damier, Philippe, Viallet, François, Houeto, Jean-Luc, Durif, Franck, Vidailhet, Marie, Worbe, Yulia, Roze, Emmanuel, Kabashi, Edor, Hartmann, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878848/
https://www.ncbi.nlm.nih.gov/pubmed/31824749
http://dx.doi.org/10.7916/tohm.v0.693

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878848/
https://www.ncbi.nlm.nih.gov/pubmed/31824749
http://dx.doi.org/10.7916/tohm.v0.693

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