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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...
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| 出版年: | Int J Mol Sci |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7727818/ https://ncbi.nlm.nih.gov/pubmed/33255508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21238922 |
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