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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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Pubblicato in:Int J Mol Sci
Autori principali: Aldaz, C. Marcelo, Hussain, Tabish
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2020
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Accesso online: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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