A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology-Reference-Cited by-同舟云学术

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A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology

Published:2014-09 Issue:9 Volume:35 Page:2180.e1-2180.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Pasanen Petra,Myllykangas Liisa,Siitonen Maija,Raunio Anna,Kaakkola Seppo,Lyytinen Jukka,Tienari Pentti J.,Pöyhönen Minna,Paetau Anders

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference25 articles.

1. Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease;Appel-Cresswell;Mov. Disord.,2013

2. Alpha-synuclein locus duplication as a cause of familial Parkinson's disease;Chartier-Harlin;Lancet,2004

3. Mutation E46K increases phospholipid binding and assembly into filaments of human alpha-synuclein;Choi;FEBS Lett.,2004

4. Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease;Conway;Nat. Med.,1998

5. Immunoreactivity profile of hippocampal CA2/3 neurites in diffuse Lewy body disease;Dickson;Acta Neuropathol.,1994

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