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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Bibliographic Details
Main Authors: Ehaideb Salleh N., Al-Bu Ali Majed J., Al-obaid Jaafer J., Aljassim Kareemah M., Alfadhel Majid
Format: Article
Language:English
Published: De Gruyter 2018-12-01
Series:Translational Neuroscience
Subjects:
Online Access:https://doi.org/10.1515/tnsci-2018-0029