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Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation

Published:September 26, 2013DOI:https://doi.org/10.1016/j.braindev.2013.09.001
      We read with great interest the article by Torisu et al. who reported “Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes” [
      • Torisu H.
      • Watanabe K.
      • Shimojima K.
      • Sugawara M.
      • Sanefuji M.
      • Ishizaki Y.
      • et al.
      Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes.
      ].
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