CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1

Tourette syndrome (TS) is a neuropsychiatric disorder with a strong genetic component. However, the genetic architecture of TS remains uncertain. Copy number variation (CNV) has been shown to contribute to the genetic make-up of several neurodevelopmental conditions, including schizophrenia and auti...

Descripción completa

Detalles Bibliográficos
Autores principales: Nag, Abhishek, Bochukova, Elena G., Kremeyer, Barbara, Campbell, Desmond D., Muller, Heike, Valencia-Duarte, Ana V., Cardona, Julio, Rivas, Isabel C., Mesa, Sandra C., Cuartas, Mauricio, Garcia, Jharley, Bedoya, Gabriel, Cornejo, William, Herrera, Luis D., Romero, Roxana, Fournier, Eduardo, Reus, Victor I., Lowe, Thomas L., Farooqi, I. Sadaf, Mathews, Carol A., McGrath, Lauren M., Yu, Dongmei, Cook, Ed, Wang, Kai, Scharf, Jeremiah M., Pauls, David L., Freimer, Nelson B., Plagnol, Vincent, Ruiz-Linares, Andrés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606459/
https://www.ncbi.nlm.nih.gov/pubmed/23533600
http://dx.doi.org/10.1371/journal.pone.0059061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606459/
https://www.ncbi.nlm.nih.gov/pubmed/23533600
http://dx.doi.org/10.1371/journal.pone.0059061

Ejemplares similares