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Original research
Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk

Authors

  • Dheeraj Reddy Bobbili Bioinformatics Core, Luxembourg Centre for Systems Biomedicine (LCSB), Belvaux, LuxembourgMeGeno S.A, Esch-sur-Alzette, Luxembourg PubMed articlesGoogle scholar articles
  • Peter Banda Bioinformatics Core, Luxembourg Centre for Systems Biomedicine (LCSB), Belvaux, Luxembourg PubMed articlesGoogle scholar articles
  • Rejko Krüger Developmental and Cellular Biology, Luxembourg Centre for Systems Biomedicine (LCSB), Belvaux, LuxembourgParkinson Research Clinic, Centre Hospitalier de Luxemborg (CHL), Luxembourg, LuxembourgTransversal Translational Medicine, Luxembourg Institute of Health (LIH), Strassen, Luxembourg PubMed articlesGoogle scholar articles
  • Patrick May Bioinformatics Core, Luxembourg Centre for Systems Biomedicine (LCSB), Belvaux, Luxembourg PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Patrick May, Bioinformatics, Luxembourg Centre for Systems Biomedicine, Belvaux, Luxembourg;; Dr Dheeraj Reddy Bobbili; dheeraj.bobbili{at}uni.lu
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Citation

Bobbili DR, Banda P, Krüger R, et al
Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk

Publication history

  • Received May 26, 2019
  • Revised December 4, 2019
  • Accepted January 20, 2020
  • First published February 13, 2020.
  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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