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Neurogenetics
KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects
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Authors

  • Chiao Xin Lim Epilepsy Research Group, School of Pharmacy and Medical Sciences, Sansom Institute for Health Research and Centre for Cancer Biology, University of South Australia, Adelaide, South Australia, Australia PubMed articlesGoogle scholar articles
  • Michael G Ricos Epilepsy Research Group, School of Pharmacy and Medical Sciences, Sansom Institute for Health Research and Centre for Cancer Biology, University of South Australia, Adelaide, South Australia, Australia PubMed articlesGoogle scholar articles
  • Leanne M Dibbens Epilepsy Research Group, School of Pharmacy and Medical Sciences, Sansom Institute for Health Research and Centre for Cancer Biology, University of South Australia, Adelaide, South Australia, Australia PubMed articlesGoogle scholar articles
  • Sarah E Heron Epilepsy Research Group, School of Pharmacy and Medical Sciences, Sansom Institute for Health Research and Centre for Cancer Biology, University of South Australia, Adelaide, South Australia, Australia PubMed articlesGoogle scholar articles
  1. 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
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Citation

Lim CX, Ricos MG, Dibbens LM, et al
KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects
Journal of Medical Genetics 2016;53:217-225.

Publication history

  • Received September 9, 2015
  • Revised December 1, 2015
  • Accepted December 6, 2015
  • First published January 6, 2016.
Online issue publication 
February 09, 2017

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