FBXO7 mutations in Parkinson's disease and multiple system atrophy-Reference-Cited by-同舟云学术

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FBXO7 mutations in Parkinson's disease and multiple system atrophy

Published:2016-04 Issue: Volume:40 Page:192.e1-192.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Conedera Silvio,Apaydin Hulya,Li Yuanzhe,Yoshino Hiroyo,Ikeda Aya,Matsushima Takashi,Funayama Manabu,Nishioka Kenya,Hattori Nobutaka

Funder

JSPS

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference17 articles.

1. The Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagy;Burchell;Nat. Neurosci.,2013

2. What genetics tells us about the causes and mechanisms of Parkinson's disease;Corti;Physiol. Rev.,2011

3. F-box only protein 7 gene in parkinsonian-pyramidal disease;Deng;JAMA Neurol.,2013

4. FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome;Di Fonzo;Neurology,2009

5. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism;Edvardson;PLoS One,2012

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