Mutations in ATXN2, the gene encoding ataxin 2 — an RNA-binding protein found throughout the body with multiple roles in RNA metabolism — have been implicated in both amyotrophic lateral sclerosis (ALS) and spinocerebellar ataxia type 2 (SCA2). Writing in Nature, two new

中文翻译：

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神经退行性疾病：减少Ataxin 2可以挽救运动缺陷

ATXN2突变是编码共济失调蛋白2的基因（一种在人体中发现的在RNA代谢中具有多种作用的RNA结合蛋白），已与肌萎缩性侧索硬化症（ALS）和2型小脑脊髓共济失调（SCA2）有关。《自然写作》中的两个新内容