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Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder
Bipolar disorder affects about 1% of the world's population, and its estimated heritability is about 75%. Only few whole genome or whole-exome sequencing studies in bipolar disorder have been reported, and no rare coding variants have yet been robustly identified. The use of isolated population...
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| Veröffentlicht in: | Transl Psychiatry |
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Nature Publishing Group
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438033/ https://ncbi.nlm.nih.gov/pubmed/28195573 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/tp.2017.3 |
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