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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2013
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3606459/
https://ncbi.nlm.nih.gov/pubmed/23533600
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0059061
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items