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507. Association of NRXN3 deletion with schizophrenia and bipolar disorder

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dc.creatorShavit, Ayal
dc.creatorGonzalez, Jessica
dc.creatorChavez, Maricela
dc.creatorRodriguez, Marco A.
dc.creatorCamarillo, Cynthia
dc.creatorRamírez, Mercedez Ellis
dc.creatorZavala, Juan Manuel
dc.creatorContreras Rojas, Javier
dc.creatorRaventós Vorst, Henriette
dc.creatorFlores, Deborah Lynne
dc.creatorJerez Magaña, Álvaro Antonio
dc.creatorOntiveros Sánchez de la Barquera, José Alfonso
dc.creatorNicolini Sánchez, José Humberto
dc.creatorEscamilla, Michael A.
dc.creatorGonzalez, Suzanne
dc.date.accessioned2024-11-26T14:38:31Z
dc.date.available2024-11-26T14:38:31Z
dc.date.issued2017-05-17
dc.description.abstractSchizophrenia (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.
dc.description.procedenceUCR::Vicerrectoría de Docencia::Ciencias Básicas::Facultad de Ciencias::Escuela de Biología
dc.description.procedenceUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Biología Celular y Molecular (CIBCM)
dc.identifier.doihttps://doi.org/10.1016/j.biopsych.2017.02.1115
dc.identifier.issn0006-3223
dc.identifier.issn1873-2402
dc.identifier.urihttps://hdl.handle.net/10669/100136
dc.language.isoeng
dc.rightsacceso restringido
dc.sourceBiological Psychiatry, 81(S10), S206
dc.subjectSchizophrenia
dc.subjectBipolar Disorder
dc.subjectNRXN3
dc.title507. Association of NRXN3 deletion with schizophrenia and bipolar disorder
dc.typeactas de congreso

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