Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions

OBJECTIVE: Hexanucleotide repeat expansions (HREs) in C9orf72 are a major cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). We aimed to determine the frequency and phenomenology of movement disorders (MD) in carriers of HRE in C9orf72 through a retrospective review of p...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Neurol Genet
Prif Awduron: Estevez-Fraga, Carlos, Magrinelli, Francesca, Hensman Moss, Davina, Mulroy, Eoin, Di Lazzaro, Giulia, Latorre, Anna, Mackenzie, Melissa, Houlden, Henry, Tabrizi, Sarah J., Bhatia, Kailash P.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Wolters Kluwer 2021
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC8105892/
https://ncbi.nlm.nih.gov/pubmed/33977144
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000575
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