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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...
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| Publicado no: | Transl Neurosci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
De Gruyter
2018
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| Assuntos: | |
| Acesso em linha: | 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 |
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