507. Association of NRXN3 deletion with schizophrenia and bipolar disorder

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Podrobná bibliografie
Autoři:	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
Médium:	actas de congreso
Datum vydání:	2017
Popis:	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.
Země:	Kérwá
Instituce:	Universidad de Costa Rica
Repositorio:	Kérwá
Jazyk:	Inglés
OAI Identifier:	oai:kerwa.ucr.ac.cr:10669/100136
On-line přístup:	https://hdl.handle.net/10669/100136 https://doi.org/10.1016/j.biopsych.2017.02.1115
Klíčové slovo:	Schizophrenia Bipolar Disorder NRXN3