神经科学
肌萎缩侧索硬化
物理医学与康复
医学
心理学
疾病
内科学
作者
Cathrine Goberg Olsen,Øyvind L. Busk,Øystein L. Holla,Kristian Tveten,Trygve Holmøy,Ole‐Bjørn Tysnes,Helle Høyer
标识
DOI:10.1080/21678421.2023.2270705
摘要
In Norway, 89% of patients with Amyotrophic lateral sclerosis (ALS) lacks a genetic diagnose. ALS genes and genes that cause other neuromuscular or neurodegenerative disorders extensively overlap. This population-based study examined whether patients with ALS have a family history of neurological disorders and explored the occurrence of rare genetic variants associated with other neurodegenerative or neuromuscular disorders.
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