CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1
ABSTRACT: 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 schizophreni...
- Autores:
-
Nag, Abhishek
Bochukova, Elena
Kremeyer, Barbara Kremeyer
Campbell, Desmond
Muller, Heike
Valencia Duarte, Ana Victoria
Cardona Silgado, Julio Cesar
Rivas, Isabel Cristina
Mesa Restrepo, Sandra Catalina
Cuartas Arias, Jorge Mauricio
García Cerén, Jharley Jair
Bedoya Berrío, Gabriel De Jesús
Cornejo Ochoa, José William
Herrera Amighetti, Luis Diego
Romero, Roxana
Fournier, Eduardo
Reus, Victor
Lowe, Thomas
Farooqi, Ismaa Sadaf
Mathews, Carol
McGrath, Lauren
Yu, Dongmei
Cook, Ed
Wang, Kai
Scharf, Jeremiah
Pauls, David
Freimer, Nelson
Plagnol, Vincent
Ruíz Linares, Andrés
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2013
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/23730
- Acceso en línea:
- http://hdl.handle.net/10495/23730
- Palabra clave:
- Síndrome de Tourette
Tourette Syndrome
Trastornos del Neurodesarrollo
Neurodevelopmental Disorders
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/