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...

詳細記述

保存先:
書誌詳細
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: S. Karger AG 2011
主題:
Original Research Article
オンライン･アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料