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Rare disease
Case report
Novel missense mutation in the ATP1A2 gene associated with atypical sporadic hemiplegic migraine

Authors

  1. Correspondence to Dr Vincenzo Di Stefano; vincenzo19689{at}gmail.com
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Citation

Rispoli MG, Di Stefano V, Mantuano E, et al
Novel missense mutation in the ATP1A2 gene associated with atypical sporadic hemiplegic migraine
BMJ Case Reports CP 2019;12:e231129.

Publication history

  • Accepted September 18, 2019
  • First published October 5, 2019.
Online issue publication 
October 05, 2019

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© BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.