肌萎缩侧索硬化
医学
队列
内科学
生命银行
人口
疾病
逻辑回归
比例危险模型
外显子组
队列研究
肿瘤科
外显子组测序
生物信息学
遗传学
突变
生物
基因
环境卫生
作者
Erin N. Smith,Jonghun Lee,Daria Prilutsky,Stephen Zicha,Zemin Wang,Steve Han,Neta Zach
标识
DOI:10.1080/21678421.2023.2285428
摘要
Objective Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative disease with profound unmet need. In patients carrying genetic mutations, elevations in neurofilament light (NfL) have been shown to precede symptom onset, however, the natural history of NfL in general ALS patients is less characterized.
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