Erratum: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
In: Nature Genetics, Jg. 49 (2017-06-01), S. 969-969
Online
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Zugriff:
Nat. Genet. 49, 223–237 (2017); published online 19 December 2016; corrected after print 20 April 2017 Following publication of this article, the authors were asked to remove a clinical image and some video footage of one of the affected individuals. Although consent was obtained, in keeping with their ethical consent framework, the authors allow for withdrawal of consent and are carrying out the wishes of the research subjects under their consent process.
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Erratum: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
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Autor/in / Beteiligte Person: | Meyer, Esther ; Kurian, Manju A. ; Bhate, Sanjay ; Lin, Jean-Pierre ; Agnel Praveen Joseph ; Barnicoat, Angela ; F. Lucy Raymond ; Chubb, Jonathan R. ; Darin, Niklas ; Misra, Shibalik ; Carr, Lucinda ; Ng, Joanne ; Morrogh, Deborah ; Rankin, Julia ; Houlden, Henry ; Kamsteeg, Erik-Jan ; Smith, Martin ; Limousin, Patricia ; McKee, Shane ; Arkadir, David ; Wiethoff, Sarah ; Ben-Pazi, Hilla ; Rump, Patrick ; Chong, Wui K. ; John M.E. Nichols ; Michèl A.A.P. Willemsen ; Gahl, William A. ; Peters, Gregory ; Grozeva, Detelina ; Heales, S ; Toro, Camilo ; Reis, André ; Shekeeb S Mohammed ; Pope, Simon ; Deciphering Developmental Disorders Study ; Ngoh, Adeline ; Nicolai, Joost ; Israel, Zvi ; Dale, Russell C. ; Wood, Nicholas W. ; Barral, Serena ; Mencacci, Niccolo E. ; Wieczorek, Dagmar ; Pall, Hardev ; Winter, Gidon ; Nakou, Vasiliki ; Turnpenny, Peter D. ; Prabhakar, Prab ; Bhatia, Kailash P. ; Pittman, Alan ; Sinnema, Margje ; Wragg, Christopher ; Carss, Keren J. ; Topf, Maya ; Boys, Amber ; Papandreou, Apostolos ; Bergman, Hagai ; Segel, Reeval ; Hurst, Jane A. ; White, Susan M. ; Gutowski, Nicholas ; Hills, A. ; Kaminska, Margaret ; Lumsden, Daniel E. ; Pérez-Dueñas, Belén ; Foulds, Nicola ; Peall, Kathryn J. ; Gissen, Paul ; Reuter, Miriam S. ; Nilsson, Magnus ; Wilson, Brian T. |
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Zeitschrift: | Nature Genetics, Jg. 49 (2017-06-01), S. 969-969 |
Veröffentlichung: | Springer Science and Business Media LLC, 2017 |
Medientyp: | unknown |
ISSN: | 1546-1718 (print) ; 1061-4036 (print) |
DOI: | 10.1038/ng0617-969b |
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