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Article

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

Neurology - 23 Apr 2002

Janssen J C, Warrington E K, Morris H R, Lantos P, Brown J, Revesz T, Wood N, Khan M N, Cipolotti L, Fox N C, Rossor M N

Abstract excerpt

OBJECTIVE: To describe the clinical features of nine British families with neuropathologically verified frontotemporal dementia (FTD) due to the intronic tau exon 10(+16) mutation. METHODS: Retrospective chart reviews of family members with FTD belonging to nine tau 10(+16) mutation pedigrees in whom neuropathologic examination had been carried out. APOE genotype was determined for those patients for whom DNA was...

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Identifiers

PMID: 11971081
DOI: 10.1212/wnl.58.8.1161

Genes

APOE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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