Unravelling the clinical spectrum and the role of repeat length in C9ORF72 repeat expansions

Since the discovery of the C9orf72 repeat expansion as the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis, it has increasingly been associated with a wider spectrum of phenotypes, including other types of dementia, movement disorders, psychiatric symptom...

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Bibliographic Details
Published in:J Neurol Neurosurg Psychiatry
Main Authors: van der Ende, Emma L., Jackson, Jazmyne L., White, Adrianna, Seelaar, Harro, van Blitterswijk, Marka, Van Swieten, John C.
Format: Artigo
Language:Inglês
Published: BMJ Publishing Group 2021
Subjects:
Neurodegeneration
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC8053328/
https://ncbi.nlm.nih.gov/pubmed/33452054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp-2020-325377
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