Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations-Reference-Cited by-同舟云学术

Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations

Published:2017-12-20 Issue:2 Volume:77 Page:128-138
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:

Author:

Ayaki Takashi,Ito Hidefumi,Komure Osamu,Kamada Masaki,Nakamura Masataka,Wate Reika,Kusaka Hirofumi,Yamaguchi Yuko,Li Fangzhou,Kawakami Hideshi,Urushitani Makoto,Takahashi Ryosuke

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://academic.oup.com/jnen/article-pdf/77/2/128/23373425/nlx109.pdf

Reference28 articles.

1. Mutations of optineurin in amyotrophic lateral sclerosis;Nature,2010

2. Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease;Acta Neuropathol,2015

3. Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation;Acta Neuropathol,2011

4. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation;Neuropathology,2014

5. Isoform transition from four-repeat to three-repeat tau underlies dendrosomatic and regional progression of neurofibrillary pathology;Acta Neuropathol,2013

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