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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...

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Vydáno v:	Neurol Genet
Hlavní autoři:	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.
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wolters Kluwer 2021
Témata:	Article
On-line přístup:	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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Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions

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