Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Nat Genet
.
2017 May 26;49(6):969.
doi: 10.1038/ng0617-969b.
Authors
Esther Meyer
,
Keren J Carss
,
Julia Rankin
,
John M E Nichols
,
Detelina Grozeva
,
Agnel P Joseph
,
Niccolo E Mencacci
,
Apostolos Papandreou
,
Joanne Ng
,
Serena Barral
,
Adeline Ngoh
,
Hilla Ben-Pazi
,
Michel A Willemsen
,
David Arkadir
,
Angela Barnicoat
,
Hagai Bergman
,
Sanjay Bhate
,
Amber Boys
,
Niklas Darin
,
Nicola Foulds
,
Nicholas Gutowski
,
Alison Hills
,
Henry Houlden
,
Jane A Hurst
,
Zvi Israel
,
Margaret Kaminska
,
Patricia Limousin
,
Daniel Lumsden
,
Shane McKee
,
Shibalik Misra
,
Shekeeb S Mohammed
,
Vasiliki Nakou
,
Joost Nicolai
,
Magnus Nilsson
,
Hardev Pall
,
Kathryn J Peall
,
Gregory B Peters
,
Prab Prabhakar
,
Miriam S Reuter
,
Patrick Rump
,
Reeval Segel
,
Margje Sinnema
,
Martin Smith
,
Peter Turnpenny
,
Susan M White
,
Dagmar Wieczorek
,
Sarah Wiethoff
,
Brian T Wilson
,
Gidon Winter
,
Christopher Wragg
,
Simon Pope
,
Simon J H Heales
,
Deborah Morrogh
;
UK10K Consortium
;
Deciphering Developmental Disorders Study
;
NIHR BioResource Rare Diseases Consortium
;
Alan Pittman
,
Lucinda J Carr
,
Belen Perez-Dueñas
,
Jean-Pierre Lin
,
Andre Reis
,
William A Gahl
,
Camilo Toro
,
Kailash P Bhatia
,
Nicholas W Wood
,
Erik-Jan Kamsteeg
,
Wui K Chong
,
Paul Gissen
,
Maya Topf
,
Russell C Dale
,
Jonathan R Chubb
,
F Lucy Raymond
,
Manju A Kurian
PMID:
28546572
DOI:
10.1038/ng0617-969b
No abstract available
Publication types
Published Erratum
Grants and funding
G-1107/PUK_/Parkinson's UK/United Kingdom
MR/K02342X/1/MRC_/Medical Research Council/United Kingdom