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PRRT2 gene mutations From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine
Alice R. Gardiner, Kailash P. Bhatia, Maria Stamelou, Russell C. Dale, Manju A. Kurian, Susanne A. Schneider, G. M. Wali, Tim Counihan, Anthony H. Schapira, Sian D. Spacey, Enza Maria Valente, Laura Silveira-Moriyama, Hélio A.G. Teive, Salmo Raskin, Josemir W. Sander, Andrew Lees, Tom Warner, Dimitri M. Kullmann, Nicholas W. Wood, Michael Hanna
*Corresponding author for this work
- Department of Molecular Neuroscience
- Reta Lila Weston Laboratories
- MRC Centre for Neuromuscular Diseases
- University of London
- Institute of Neuroscience and Muscle Research
- University of Sydney
- Neurosciences Unit
- KLE Society Hospital
- Department of Neurology
- National University of Ireland Galway
- Division of Neurology
- University of British Columbia
- Regional General Hospital
- Movement Disorders Unit
- Federal University of Paraná
- Department of Clinical and Experimental Epilepsy
- Department of Neurology
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