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Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
The 22q11.2 deletion is a strong, but insufficient, “first hit” genetic risk factor for schizophrenia (SZ). We attempted to identify “second hits” from the entire genome in a unique multiplex 22q11.2 deletion syndrome (DS) family. Bioinformatic analysis of whole-exome sequencing and comparative-geno...
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| 出版年: | Transl Psychiatry |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group UK
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6358611/ https://ncbi.nlm.nih.gov/pubmed/30710087 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41398-018-0354-9 |
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