CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis

Although bipolar disorder is highly heritable, the identification of specific genetic variations is limited because of the complex traits underlying the disorder. We performed a genome-wide association study of bipolar disorder using a subphenotype that shows hypersomnia symptom during a major depre...

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Detalles Bibliográficos
Autores principales: Cho, Chul-Hyun, Lee, Heon-Jeong, Woo, Hyun Goo, Choi, Ji-Hye, Greenwood, Tiffany A., Kelsoe, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neuropsychiatric Association 2015
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504925/
https://www.ncbi.nlm.nih.gov/pubmed/26207136
http://dx.doi.org/10.4306/pi.2015.12.3.402

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504925/
https://www.ncbi.nlm.nih.gov/pubmed/26207136
http://dx.doi.org/10.4306/pi.2015.12.3.402

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