Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease-Reference-Cited by-同舟云学术

Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease

Published:2018-09-05 Issue:10 Volume:33 Page:1591-1600
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Gaare Johannes J.¹²^ORCID,Nido Gonzalo S.¹²,Sztromwasser Paweł³⁴⁵,Knappskog Per M.³⁶,Dahl Olav²⁷,Lund-Johansen Morten²⁸,Maple-Grødem Jodi⁹¹⁰,Alves Guido⁹¹¹¹²,Tysnes Ole-Bjørn¹²,Johansson Stefan³⁶,Haugarvoll Kristoffer¹²^ORCID,Tzoulis Charalampos¹²^ORCID

Affiliation:

1. Department of Neurology; Haukeland University Hospital; Bergen Norway

2. Department of Clinical Medicine; University of Bergen; Bergen Norway

3. Center for Medical Genetics and Molecular Medicine; Haukeland University Hospital; Bergen Norway

4. Department of Clinical Science; University of Bergen; Bergen Norway

5. Computational Biology Unit, Department of Informatics; University of Bergen; Bergen Norway

6. K.G. Jebsen Centre for Neuropsychiatric Disorders, Department of Clinical Science; University of Bergen; Bergen Norway

7. Department of Oncology; Haukeland University Hospital; Bergen Bergen Norway

8. Department of Neurosurgery; Haukeland University Hospital; Bergen Bergen Norway

9. The Norwegian Centre for Movement Disorders; Stavanger University Hospital; Stavanger Norway

10. Centre for Organelle Research; University of Stavanger; Stavanger Norway

11. Department of Neurology; Stavanger University Hospital; Stavanger Norway

12. Department of Mathematics and Natural Sciences; University of Stavanger; Stavanger Norway

Funder

Regional Health Authority of Western Norway

Norges Forskningsråd

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.64/fullpdf

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5. DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy;Thomas;Hum Mol Genet,2011

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