Neonatal neuronal WWOX gene therapy rescues Wwox null phenotypes
Abstract WW domain‐containing oxidoreductase (WWOX) is an emerging neural gene‐regulating homeostasis of the central nervous system. Germline biallelic mutations in WWOX cause WWOX‐related epileptic encephalopathy (WOREE) syndrome and spinocerebellar ataxia and autosomal recessive 12 (SCAR12), two d...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer Nature
2021-11-01
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| Sarja: | EMBO Molecular Medicine |
| Aiheet: | |
| Linkit: | https://doi.org/10.15252/emmm.202114599 |
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