VPS35 mutation in Japanese patients with typical Parkinson's disease-Reference-Cited by-同舟云学术

VPS35 mutation in Japanese patients with typical Parkinson's disease

Published:2012-09-15 Issue:11 Volume:27 Page:1413-1417
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Ando Maya,Funayama Manabu,Li Yuanzhe,Kashihara Kenichi,Murakami Yoshitake,Ishizu Nobutaka,Toyoda Chizuko,Noguchi Katsuhiko,Hashimoto Takashi,Nakano Naoki,Sasaki Ryogen,Kokubo Yasumasa,Kuzuhara Shigeki,Ogaki Kotaro,Yamashita Chikara,Yoshino Hiroyo,Hatano Taku,Tomiyama Hiroyuki,Hattori Nobutaka

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25145/fullpdf

Reference25 articles.

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2. Parkinson's disease: from monogenic forms to genetic susceptibility factors;Lesage;Hum Mol Genet,2009

3. VPS35 mutations in Parkinson disease;Vilariño-Güell;Am J Hum Genet,2011

4. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease;Zimprich;Am J Hum Genet,2011

5. Retromer;Bonifacino;Retromer. Curr Opin Cell Biol,2008

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