Articles with "c9orf72 expansions" as a keyword



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C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort

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Published in 2023 at "Annals of Clinical and Translational Neurology"

DOI: 10.1002/acn3.51744

Abstract: Frontotemporal dementia (FTD) encompasses a spectrum of neurodegenerative disorders, including behavioural variant FTD (bvFTD), semantic variant primary progressive aphasia (svPPA) and non‐fluent variant PPA (nfvPPA). While a strong genetic component is implicated in FTD, genetic… read more here.

Keywords: southeast asian; frontotemporal dementia; c9orf72 expansions; ftd ... See more keywords