An autopsied FTDP-17 case with MAPT IVS 10 + 14C > T mutation presenting with frontotemporal dementia-Reference-Cited by-同舟云学术

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An autopsied FTDP-17 case with MAPT IVS 10 + 14C > T mutation presenting with frontotemporal dementia

Published:2021-09 Issue: Volume:24 Page:100363
ISSN:2405-6502
Container-title:eNeurologicalSci
language:en
Short-container-title:eNeurologicalSci

Author:

Watanabe Ryohei,Kawakami Ito,Ikeuchi Takeshi,Murayama Shigeo,Arai Tetsuaki,Akiyama Haruhiko,Onaya Mitsumoto,Hasegawa Masato

Funder

Japan Agency for Medical Research and Development

Japan Science and Technology Agency

Naito Foundation

Publisher

Elsevier BV

Subject

Neurology

Reference10 articles.

1. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex;Lynch;Neurology,1994

2. Tau mutations in frontotemporal dementia FTDP-17 and their relevance for Alzheimer’s disease;Goedert;Biochim. Biophys. Acta,2000

3. Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging;Ghetti;Neuropathol. Appl. Neurobiol.,2015

4. Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies;Forrest;Brain,2018

5. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia;Rascovsky;Brain,2011

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