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Article

A novel MAPT mutation (P301T) associated with familial frontotemporal dementia.

European journal of neurology - 1 Aug 2007

Lladó A, Ezquerra M, Sánchez-Valle R, Rami L, Tolosa E, Molinuevo J L

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Source

Identifiers

PMID: 17662000
DOI: 10.1111/j.1468-1331.2007.01763.x

Genes

MAPT

Variants

Provenance

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Related research

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Research trail→

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A novel MAPT mutation (P301T) associated with familial frontotemporal dementia.PMID 17662000Read ↗

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.Semantic proximity Read ↗

Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia.Semantic proximity Read ↗

de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia.Semantic proximity Read ↗

Clinical and neuroimaging characterization of the first frontotemporal dementia family carrying the MAPT p.K298E mutation.Semantic proximity Read ↗

New MAPT variant in a FTD patient with Alzheimer's disease phenotype at onset.Semantic proximity Read ↗

Frontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, Spain.Semantic proximity Read ↗

Clinical, neuropathological, and biochemical characterization of the novel tau mutation P332S.Semantic proximity Read ↗

Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation.Semantic proximity Read ↗

A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.Semantic proximity Read ↗

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutationSemantic proximity Read ↗

Identification and functional characterization of novel variants of MAPT and GRN in Chinese patients with frontotemporal dementia.Semantic proximity Read ↗

Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.Semantic proximity Read ↗

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