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Original article
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene
  1. Correspondence to Professor Anna-Elina Lehesjoki, Folkhälsan Institute of Genetics, Biomedicum Helsinki, PO Box 63 (Haartmaninkatu 8), University of Helsinki, FIN-00014 Helsinki, Finland; anna-elina.lehesjoki{at}helsinki.fi
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Citation

Kousi M, Anttila V, Schulz A, et al
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Publication history

  • Received March 1, 2012
  • Revised April 16, 2012
  • Accepted April 18, 2012
  • First published June 12, 2012.
Online issue publication 
June 12, 2012

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