Evidence for a Common Founder and Clinical Characteristics of Japanese Families with the MAPT R406W Mutation

BACKGROUND/AIM: Mutations in MAPT cause frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17). Patients with the MAPT R406W mutation were reported to show phenotypic heterogeneity in different ethnic backgrounds. We here report the clinical and genetic characteristics of Japane...

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Detalhes bibliográficos
Main Authors: Ikeuchi, Takeshi, Imamura, Toru, Kawase, Yasuhiro, Kitade, Yoshimi, Tsuchiya, Miyuki, Tokutake, Takayoshi, Kasuga, Kensaku, Yajima, Ryuji, Tsukie, Tamao, Miyashita, Akinori, Sugishita, Morihiro, Kuwano, Ryozo, Nishizawa, Masatoyo
Formato: Artigo
Idioma:Inglês
Publicado em: S. Karger AG 2011
Assuntos:
Original Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3235940/
https://ncbi.nlm.nih.gov/pubmed/22545037
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000331243
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