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Article

Phenotypic heterogeneity within a new family with the MAPT p301s mutation.

Annals of neurology - 1 Dec 2005

Yasuda Minoru, Nakamura Yoshitsugu, Kawamata Toshio, Kaneyuki Hiroshi, Maeda Kiyoshi, Komure Osamu

Abstract excerpt

Mutations in the gene encoding the microtubule-associated protein tau (MAPT) cause frontotemporal dementia and parkinsonism linked to chromosome 17. Clinical variability is seen not only among families with different mutations, but also among family members with the same mutation. We investigated...

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Identifiers

PMID: 16240366
DOI: 10.1002/ana.20668

Genes

MAPT

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16240366-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Phenotypic heterogeneity within a new family with the MAPT p301s mutation.PMID 16240366Read ↗

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