Associated Papers
C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort.
Tan YJ et al.
Annals of Clinical and Translational Neurology, 2023
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
Chiang HH et al.
European Journal of Human Genetics : Ejhg, 2013
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