Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.

Journal of neural transmission (Vienna, Austria : 1996) - 1 Jul 2007

Baba Y, Baker M C, Le Ber I, Brice A, Maeck L, Kohlhase J, Yasuda M, Stoppe G, Bugiani O, Sperfeld A D, Tsuboi Y, Uitti R J, Farrer M J, Ghetti B, Hutton M L, Wszolek Z K

Abstract excerpt

In 9 patients with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) with a P301S tau mutation, the predominant phenotype was frontotemporal dementia in 3 and parkinsonism in 6. Comparison of the tau genotype/haplotype carrying the mutation and the initial clinical sign s...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Pair 17
Share to Frontotemporal Lobar Degeneration

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Linkage

Share to Genotype

Share to Haplotypes

Share to Parkinsonian Disorders

Share to tau Proteins

Share to Young Adult

Source

Identifiers

PMID: 17318302
DOI: 10.1007/s00702-007-0632-9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17318302-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation.PMID 17318302Read ↗

The effect of tau genotype on clinical features in FTDP-17.Semantic proximity Read ↗

Tau gene mutations and tau pathology in frontotemporal dementia and parkinsonism linked to chromosome 17.Semantic proximity Read ↗

Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17.Semantic proximity Read ↗

Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family.Semantic proximity Read ↗

Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17.Semantic proximity Read ↗

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).Semantic proximity Read ↗

Association between the extended tau haplotype and frontotemporal dementia.Semantic proximity Read ↗

Molecular genetics of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).Semantic proximity Read ↗

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.Semantic proximity Read ↗

MAPT mutation associated with frontotemporal dementia and parkinsonism (FTDP-17).Semantic proximity Read ↗

The tau H1 haplotype is associated with Parkinson's disease in the Norwegian population.Semantic proximity Read ↗

Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.