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WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders
The WWOX gene was initially discovered as a putative tumor suppressor. More recently, its association with multiple central nervous system (CNS) pathologies has been recognized. WWOX biallelic germline pathogenic variants have been implicated in spinocerebellar ataxia type 12 (SCAR12; MIM:614322) an...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727818/ https://www.ncbi.nlm.nih.gov/pubmed/33255508 http://dx.doi.org/10.3390/ijms21238922 |