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Movement disorders
Short Report
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene

Authors

  1. Correspondence to Dr Agathe Roubertie, Service de Neuropédiatrie, CHU Gui de Chauliac, 80 Avenue Fliche, Montpellier 34295, France; A-roubertie{at}chu-montpellier.fr
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Citation

Delcourt M, Riant F, Mancini J, et al
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene
Journal of Neurology, Neurosurgery & Psychiatry 2015;86:782-785.

Publication history

  • Received July 18, 2014
  • Revised October 16, 2014
  • Accepted October 17, 2014
  • First published January 16, 2015.
Online issue publication 
April 16, 2018

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