507. Association of NRXN3 deletion with schizophrenia and bipolar disorder

 

שמור ב:
מידע ביבליוגרפי
Autores: 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
פורמט: actas de congreso
Fecha de Publicación:2017
תיאור: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.
País:Kérwá
מוסד:Universidad de Costa Rica
Repositorio:Kérwá
שפה:Inglés
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/100136
גישה מקוונת:https://hdl.handle.net/10669/100136
https://doi.org/10.1016/j.biopsych.2017.02.1115
מילת מפתח:Schizophrenia
Bipolar Disorder
NRXN3

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