Differences in Motor Features of C9orf72, MAPT, or GRN Variant Carriers With Familial Frontotemporal Lobar Degeneration
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DOI: 10.1212/wnl.0000000000200860
Abstract: Background and Objectives Familial frontotemporal lobar degeneration (f-FTLD) is a phenotypically heterogeneous spectrum of neurodegenerative disorders most often caused by variants within chromosome 9 open reading frame 72 (C9orf72), microtubule-associated protein tau (MAPT), or granulin… read more here.
Keywords: c9orf72 mapt; frontotemporal lobar; grn; lobar degeneration ... See more keywords