SCFD1 in amyotrophic lateral sclerosis:reconciling a genetic association with in vivo functional analysis
Ruben J.Cauchi
Centre for Molecular Medicine and Biobanking,Biomedical Sciences Building;Department of Physiology and Biochemistry,Faculty of Medicine and Surgery,University of Malta,Msida,Malta
摘要：Amyotrophic lateral sclerosis(ALS)is a neurodegenerative disease characterized by progressive loss of upper and lower motor neurons,resulting in muscle weakness and spasticity,eventually leading to death due to respiratory failure.Analyses by our group of a case-control cohort from an isolated island population have found that genetics plays a significant role in disease etiology(Farrugia Wismayer et al.,2023).
机标关键词：associationanalysisgeneticwithvivoamyotrophicfunctionallateral
论文发表日期：2024-06-28
在线出版日期：2025-08-15（本平台首次上网日期，不代表文献的发表时间）
页数：2( 1201-1202 )