Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

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@article{Meyer2017MutationsIT, title={Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.}, author={Esther Meyer and Keren J. Carss and Julia Rankin and John M E Nichols and Detelina Grozeva and Agnel Praveen Joseph and Niccolo E Mencacci and Apostolos Papandreou and Joanne Y W Ng and Serena Barral and Adeline Ngoh and Hilla Ben-Pazi and Mich{\`e}l A. A. P. Willemsen and David Arkadir and Angela J Barnicoat and Hagai Bergman and Sanjay Bhate and Amber Boys and Niklas Dar{\'i}n and Nicola C. Foulds and Nicholas J. Gutowski and Alison Hills and Henry Houlden and Jane A. Hurst and Zvi Israel and Margaret Kaminska and Patricia Limousin and Daniel E Lumsden and Margo Whiteford and Shibalik Misra and Shekeeb S Mohammed and Vasiliki Nakou and Joost Nicolai and Magnus Nilsson and Hardev Singh Pall and Kathryn J Peall and Gregory B. Peters and Prab Prabhakar and Miriam S Reuter and Patrick Rump and Reeval Segel and Margje Sinnema and Martin Smith and Peter D. Turnpenny and Susan M White and Dagmar Wieczorek and Sarah Wiethoff and Brian T Wilson and Gidon N Winter and Christopher Wragg and Simon A. Pope and Simon J H Heales and Deborah Morrogh and Alan M. Pittman and Lucinda J Carr and Bel{\'e}n P{\'e}rez-Due{\~n}as and Jean-Pierre Lin and Andr{\'e} Reis and William A Gahl and Camilo Gonz{\'a}lez Toro and Kailash P Bhatia and Nicholas W. Wood and Erik-Jan Kamsteeg and Wui Khean Kling Chong and Paul Gissen and Maya Topf and Russell C Dale and Jonathan R Chubb and FLucy Raymond and Manju A. Kurian}, journal={Nature genetics}, year={2017}, volume={49 2}, pages={223-237} }