Article info

Download PDFPDF

Letter
A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers

Authors

  1. Correspondence to Professor Anthony H V Schapira, Department of Clinical Neurosciences, Rowland Hill St., London NW3 2PF, UK; a.schapira{at}ucl.ac.uk
View Full Text

Citation

McNeill A, Duran R, Hughes DA, et al
A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers

Publication history

  • Received January 30, 2012
  • Revised March 12, 2012
  • Accepted March 29, 2012
  • First published May 10, 2012.
Online issue publication 
July 10, 2012

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.