Article info
Review
Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy
- Correspondence to Dr Sarah E Heron, School of Pharmacy and Medical Sciences, University of South Australia, P4-47, City East Campus, GPO Box 2471, Adelaide, SA 5001, Australia; sarah.heron{at}unisa.edu.au
Citation
Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy
Publication history
- Received November 7, 2012
- Revised December 18, 2012
- Accepted December 20, 2012
- First published January 23, 2013.
Online issue publication
February 13, 2013
Article Versions
- Previous version (23 January 2013).
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