Young Onset Alzheimer’s Disease Associated with <i>C9ORF72</i> Hexanucleotide Expansion: Further Evidence for a Still Unsolved Association

Young Onset Alzheimer’s Disease Associated with <i>C9ORF72</i> Hexanucleotide Expansion: Further Evidence for a Still Unsolved Association

Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are recognized as part of a disease continuum (FTD-ALS spectrum), in which the most common genetic cause is chromosome 9 open reading frame 72 (<i>C9ORF72</i>) gene hexanucleotide repeat expansion. The clinical phenoty...

Full description

Bibliographic Details
Main Authors: Giulia Vinceti, Chiara Gallingani, Elisabetta Zucchi, Ilaria Martinelli, Giulia Gianferrari, Cecilia Simonini, Roberta Bedin, Annalisa Chiari, Giovanna Zamboni, Jessica Mandrioli
Format: Article
Language:English
Published: MDPI AG 2023-04-01
Series:Genes
Subjects:
Alzheimer’s disease
<i>C9ORF72</i>
Frontotemporal dementia
amyotrophic lateral sclerosis
Online Access:https://www.mdpi.com/2073-4425/14/4/930

Internet

https://www.mdpi.com/2073-4425/14/4/930

Similar Items