507. Association of NRXN3 deletion with schizophrenia and bipolar disorder

 

Tallennettuna:
Bibliografiset tiedot
Tekijät: Shavit, Ayal, Gonzalez, Jessica, Chavez, Maricela, Rodriguez, Marco A., Camarillo, Cynthia, Ramírez, Mercedez Ellis, Zavala, Juan Manuel, Contreras Rojas, Javier, Raventós Vorst, Henriette, Flores, Deborah Lynne, Jerez Magaña, Álvaro Antonio, Ontiveros Sánchez de la Barquera, José Alfonso, Nicolini Sánchez, José Humberto, Escamilla, Michael A., Gonzalez, Suzanne
Aineistotyyppi: actas de congreso
Julkaisupäivä:2017
Kuvaus:Schizophrenia (SZ) and bipolar disorder (BD) are the most severe neuropsychiatric disorders affecting 1.2% and 4.4% of Americans, respectively. Certain genes coding for proteins involved in pre-synaptic machinery are thought to play a role in the pathophysiology of the disorder. Deficits in the calcium channel regulator gene NRXN3 have been associated with behaviors of impulsivity and alcohol and drug dependence, which are traits characteristic of BD and SZ.
Maa:Kérwá
Organisaatio:Universidad de Costa Rica
Repositorio:Kérwá
Kieli:Inglés
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/100136
Linkit:https://hdl.handle.net/10669/100136
https://doi.org/10.1016/j.biopsych.2017.02.1115
Sanahaku:Schizophrenia
Bipolar Disorder
NRXN3