The M458L missense mutation disrupts the catalytic properties of Parkin-Reference-Cited by-同舟云学术

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The M458L missense mutation disrupts the catalytic properties of Parkin

Published:2017-12-27 Issue:1 Volume:592 Page:78-88
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:FEBS Lett

Author:

Do Yun-Ju¹,Yun Seo Young¹,Park Min-Young¹,Kim Eunhee¹

Affiliation:

1. Department of Biological Sciences; Chungnam National University; Daejeon Korea

Funder

National Research Foundation

Ministry of Science, ICT and Future Planning

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/1873-3468.12934/fullpdf

Reference66 articles.

1. Prevalence of Parkinsonism and Parkinson's disease in Europe: the EUROPARKINSON Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's disease;Rijk;J Neurol Neurosurg Psychiatry,1997

2. Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity;Hampe;Hum Mol Genet,2006

3. The genetic background of Parkinson's disease: current progress and future prospects;Kalinderi;Acta Neurol Scand,2016

4. Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease;Choi;Neurogenetics,2008

5. Distribution, type, and origin of Parkin mutations: review and case studies;Hedrich;Mov Disord,2004

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Update on the association between alpha‐synuclein and tau with mitochondrial dysfunction: Implications for Parkinson's disease;European Journal of Neuroscience;2020-02-25

2. Parkin truncating variants result in a loss-of-function phenotype;Scientific Reports;2019-11-06

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