CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.

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...

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Autores principales: Abhishek Nag, Elena G Bochukova, Barbara Kremeyer, Desmond D Campbell, Heike Muller, Ana V Valencia-Duarte, Julio Cardona, Isabel C Rivas, Sandra C Mesa, Mauricio Cuartas, Jharley Garcia, Gabriel Bedoya, William Cornejo, Luis D Herrera, Roxana Romero, Eduardo Fournier, Victor I Reus, Thomas L Lowe, I Sadaf Farooqi, Tourette Syndrome Association International Consortium for Genetics, Carol A Mathews, Lauren M McGrath, Dongmei Yu, Ed Cook, Kai Wang, Jeremiah M Scharf, David L Pauls, Nelson B Freimer, Vincent Plagnol, Andrés Ruiz-Linares
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
Medicine
R
Science
Q
Acceso en línea:https://doaj.org/article/eafb2194ce3c4fd685929f44b9c67258
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