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Short report
Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state

Authors

  1. Correspondence to Professor Knut Brockmann, University Medical Center Göttingen, Gottingen 37075, Germany; kbrock{at}med.uni-goettingen.de; Professor Bernd Wollnik; bernd.wollnik{at}med.uni-goettingen.de
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Citation

Yigit G, Sheffer R, Daana M, et al
Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state

Publication history

  • Received February 17, 2021
  • Accepted May 8, 2021
  • First published June 25, 2021.
  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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