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Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy

Authors

  1. Correspondence to Dr Ellen Knierim, Department of Neuropediatrics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, D-13353 Berlin, Germany; ellen.knierim{at}charite.de
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Citation

Rajab A, Schuelke M, Gill E, et al
Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy

Publication history

  • Received February 19, 2015
  • Revised May 14, 2015
  • Accepted May 15, 2015
  • First published June 5, 2015.
Online issue publication 
April 27, 2016

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