A NovelDCTN1mutation with late-onset parkinsonism and frontotemporal atrophy-Reference-Cited by-同舟云学术

A NovelDCTN1mutation with late-onset parkinsonism and frontotemporal atrophy

Published:2014-02-22 Issue:9 Volume:29 Page:1201-1204
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Araki Eiichi¹,Tsuboi Yoshio²,Daechsel Justus³,Milnerwood Austen⁴,Vilarino-Guell Carles⁴,Fujii Naoki¹,Mishima Takayasu²,Oka Takayuki⁵,Hara Hideo⁵,Fukae Jiro²,Farrer Matthew J.⁴

Affiliation:

1. Department of Neurology; National Omuta Hospital; Fukuoka Japan

2. Department of Neurology, Faculty of Medicine; Fukuoka University; Fukuoka Japan

3. Department of Cancer Cell Biology; Mayo Clinic; Jacksonville Florida USA

4. Department of Medical Genetics; University of British Columbia; Vancouver British Columbia Canada

5. Division of Neurology, Department of Internal Medicine; Saga University Faculty of Medicine; Saga Japan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference10 articles.

1. Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)-a literature review;Wider;Parkinsonism Relat Disord,2008

2. DCTN1 mutations in Perry syndrome;Farrer;Nat Genet,2009

3. Elucidating the genetics and pathology of Perry syndrome;Wider;J Neurol Sci,2010

4. Neurodegeneration involving putative respiratory neurons in Perry syndrome;Tsuboi;Acta Neuropathol,2008

5. Pallidonigral TDP-43 pathology in Perry syndrome;Wider;Parkinsonism Relat Disord,2009

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