Does epilepsy contribute to the clinical phenotype of C9orf72 mutation in fronto-temporal dementia?

Muroni, A; Floris, G; Polizzi, L; Fadda, L; Piga, G; Primicerio, G; Rocchi, L; Defazio, G

Muroni, A (通讯作者)，Azienda Osped Univ Cagliari, Inst Neurol, I-09042 Cagliari, Italy.

EPILEPSY & BEHAVIOR, 2022; 133 ():

Abstract

C9orf72 mutation is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) worldwide. Recently, severa......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索