Clinical and Pathological Features of FTDP‐17 with MAPT p.K298_H299insQ Mutation
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DOI: 10.1002/mdc3.14042
Abstract: MAPT is a causative gene in frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP‐17), a hereditary degenerative disease with various clinical manifestations, including progressive supranuclear palsy, corticobasal syndrome, Parkinson's disease, and frontotemporal dementia. read more here.
Keywords: k298 h299insq; features ftdp; mapt k298; clinical pathological ... See more keywords