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PDFNeurogenetics
Short report
Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state
- 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
Citation
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.
Online issue publication
November 15, 2022
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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.