Identity-by-descent analysis of a large Tourette’s syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transduction

Tourette Syndrome (TS) is a heritable, early-onset neuropsychiatric disorder that typically begins in early childhood. Identifying rare genetic variants that make a significant contribution to risk in affected families may provide important insights into the molecular aetiology of this complex and h...

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Detalles Bibliográficos
Autores principales: Ryan, Niamh, Ormond, Cathal, Chang, Yi-Chieh, Contreras, Javier, Raventos, Henriette, Gill, Michael, Heron, Elizabeth, Mathews, Carol A., Corvin, Aiden
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763103/
https://www.ncbi.nlm.nih.gov/pubmed/36224258
http://dx.doi.org/10.1038/s41380-022-01771-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763103/
https://www.ncbi.nlm.nih.gov/pubmed/36224258
http://dx.doi.org/10.1038/s41380-022-01771-9

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