Diagnostic exome sequencing in early-onset Parkinson's disease confirmsVPS13Cas a rare cause of autosomal-recessive Parkinson's disease-Reference-Cited by-同舟云学术

Diagnostic exome sequencing in early-onset Parkinson's disease confirmsVPS13Cas a rare cause of autosomal-recessive Parkinson's disease

Published:2018-01-24 Issue:3 Volume:93 Page:603-612
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Schormair B.¹²^ORCID,Kemlink D.³^ORCID,Mollenhauer B.⁴⁵,Fiala O.³⁶,Machetanz G.⁴,Roth J.³^ORCID,Berutti R.⁷,Strom T.M.²⁷,Haslinger B.⁸,Trenkwalder C.⁴,Zahorakova D.⁹^ORCID,Martasek P.⁹^ORCID,Ruzicka E.³^ORCID,Winkelmann J.¹²⁸¹⁰

Affiliation:

1. Institute of Neurogenomics; Helmholtz Zentrum München; Munich Germany

2. Institute of Human Genetics; Technische Universität München; Munich Germany

3. Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine and General University Hospital in Prague; Charles University in Prague; Prague Czech Republic

4. Paracelsus-Elena-Klinik; Kassel Germany

5. Institute of Neuropathology and Department of Neurosurgery; University Medical Center Göttingen; Göttingen Germany

6. Institute of Neuropsychiatric Care (INEP); Prague Czech Republic

7. Institute of Human Genetics; Helmholtz Zentrum München; Munich Germany

8. Neurologische Klinik und Poliklinik; Klinikum rechts der Isar der Technischen Universität München; Munich Germany

9. Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine and General University Hospital in Prague; Charles University in Prague; Prague Czech Republic

10. Munich Cluster for Systems Neurology (SyNergy); Munich Germany

Funder

Charles University Prague

Czech Ministry of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13124/fullpdf

Reference53 articles.

1. The prevalence of Parkinson's disease: a systematic review and meta-analysis;Pringsheim;Mov Disord,2014