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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Detalles Bibliográficos
Autores principales: Ehaideb, Salleh N., Al-Bu Ali, Majed J., Al-obaid, Jaafer J., Aljassim, Kareemah M., Alfadhel, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2018
Materias:
Regular Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368664/
https://www.ncbi.nlm.nih.gov/pubmed/30746283
http://dx.doi.org/10.1515/tnsci-2018-0029

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368664/
https://www.ncbi.nlm.nih.gov/pubmed/30746283
http://dx.doi.org/10.1515/tnsci-2018-0029

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