507. Association of NRXN3 deletion with schizophrenia and bipolar disorder
Kaydedildi:
| Yazarlar: | , , , , , , , , , , , , , , |
|---|---|
| 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 |