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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

  • Sarah E. Heron
  • , Bronwyn E. Grinton
  • , Sara Kivity
  • , Zaid Afawi
  • , Sameer M. Zuberi
  • , James N. Hughes
  • , Clair Pridmore
  • , Bree L. Hodgson
  • , Xenia Iona
  • , Lynette G. Sadleir
  • , James Pelekanos
  • , Eric Herlenius
  • , Hadassa Goldberg-Stern
  • , Haim Bassan
  • , Eric Haan
  • , Amos D. Korczyn
  • , Alison E. Gardner
  • , Mark A. Corbett
  • , Jozef Gécz
  • , Paul Q. Thomas
    • John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens
  • Adelaide University
  • University of Melbourne
  • Schneider Childrens Medical Center Israel
  • Tel Aviv University
  • NHS Greater Glasgow and Clyde
  • Women's and Children's Hospital Adelaide
  • University of Otago
  • University of Queensland
  • Karolinska Institutet
  • Tel Aviv Sourasky Medical Center

Research output: Contribution to journal › Article › peer-review

252 Scopus citations

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Medicine and Dentistry

Neuroscience

Biochemistry, Genetics and Molecular Biology