ロード中...
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report
BACKGROUND: The role of deleterious copy number variations in schizophrenia is well established while data regarding pathogenic variations remain scarce. We report for the first time a case of schizophrenia in a child with a pathogenic mutation of the chromodomain helicase DNA binding protein 2 (CHD...
保存先:
| 出版年: | BMC Med Genet |
|---|---|
| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2020
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6950831/ https://ncbi.nlm.nih.gov/pubmed/31914951 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0946-0 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|