載入...
Novel Homozygous Mutation in the WWOX Gene Causes Seizures and Global Developmental Delay: Report and Review
The WWOX gene has a WW domain containing oxidoreductase, which is located at the common fragile site FRA16D at chromosome 16q23. WWOX is a tumor suppressor gene that has been associated with several types of cancer such as hepatic, breast, lung, prostate, gastric, and ovarian. Recently WWOX has been...
Na minha lista:
| 發表在: | Transl Neurosci |
|---|---|
| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
De Gruyter
2018
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6368664/ https://ncbi.nlm.nih.gov/pubmed/30746283 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/tnsci-2018-0029 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|