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Original article
A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy
- Correspondence to Dr Atsushi Ishii, Department of Pediatrics, School of Medicine, Fukuoka University, 45-1, 7-chome Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan; ishii{at}fukuoka-u.ac.jp; and Dr Shinichi Hirose, Department of Pediatrics, School of Medicine, Fukuoka University, 45-1, 7-chome Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan; hirose{at}fukuoka-u.ac.jp
Citation
A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy
Publication history
- Received June 11, 2016
- Revised September 27, 2016
- Accepted September 28, 2016
- First published October 27, 2016.
Online issue publication
February 18, 2017
Article Versions
- Previous version (27 October 2016).
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/