507. Association of NRXN3 deletion with schizophrenia and bipolar disorder

 

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Detaylı Bibliyografya
Yazarlar: 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
Materyal Türü: actas de congreso
Yayın Tarihi:2017
Diğer Bilgiler: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.
Ülke:Kérwá
Kurum:Universidad de Costa Rica
Repositorio:Kérwá
Dil:Inglés
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/100136
Online Erişim:https://hdl.handle.net/10669/100136
https://doi.org/10.1016/j.biopsych.2017.02.1115
Anahtar Kelime:Schizophrenia
Bipolar Disorder
NRXN3