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  • Parkin and PINK1 mutations in early-onset Parkinson’s disease: comprehensive screening in publicly available cases and control

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Original article
Parkin and PINK1 mutations in early-onset Parkinson’s disease: comprehensive screening in publicly available cases and control

Authors

  1. Dr S W Scholz, Laboratory of Neurogenetics, National Institute on Aging, 35 Convent Drive, 20892 Bethesda, MD, USA; scholzs{at}mail.nih.gov
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Citation

Brooks J, Ding J, Simon-Sanchez J, et al
Parkin and PINK1 mutations in early-onset Parkinson’s disease: comprehensive screening in publicly available cases and control
Journal of Medical Genetics 2009;46:375-381.

Publication history

  • Received October 16, 2008
  • Revised January 1, 2009
  • Accepted January 27, 2009
  • First published April 6, 2009.
Online issue publication 
April 27, 2016

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2009 BMJ Publishing Group Ltd