C9orf72
失智症
额颞叶变性
肌萎缩侧索硬化
脑脊液
痴呆
三核苷酸重复扩增
疾病
医学
病理
遗传学
生物
基因
等位基因
作者
David Wallon,Anne Rovelet‐Lecrux,Vincent Deramecourt,Jérémie Pariente,Sophie Auriacombe,Isabelle Le Ber,Susanna Schraen‐Maschke,Florence Pasquier,Dominique Campion,Didier Hannequin
标识
DOI:10.3233/jad-2012-120877
摘要
Hexanucleotide expansion repeats in the C9ORF72 gene are a major cause of familial and, to a lesser extent, sporadic frontotemporal lobar degeneration (FTLD), amyotrophic lateral sclerosis (ALS), and FTLD-ALS. To examine whether C9ORF72 expansions co
科研通智能强力驱动
Strongly Powered by AbleSci AI