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Identification of rare non-synonymous variants in SYNE1/CPG2 in bipolar affective disorder
Bipolar affective disorder (BPD) is a severe mood disorder with a prevalence of ˜1.5% in the population. The pathogenesis of BPD is poorly understood; however, a strong heritable component has been identified. Previous genome wide association studies (GWAS) have indicated a region on 6q25, coding fo...
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| 出版年: | Psychiatr Genet |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5407451/ https://ncbi.nlm.nih.gov/pubmed/28178086 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/YPG.0000000000000166 |
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