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Mutations in the histone methyltransferase gene KMT2B cause..:
UK10K Consortium
;
Meyer, Esther
;
Carss, Keren J
...
Nature Genetics. 49 (2016) 2 - p. 223-237 , 2016
Link:
https://doi.org/10.1038/ng.3740
RT Journal T1
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_ng.3740&Exemplar=1&LAN=DE A1 UK10K Consortium A1 Meyer, Esther A1 Carss, Keren J A1 Rankin, Julia A1 Nichols, John M E A1 Grozeva, Detelina A1 Joseph, Agnel P A1 Mencacci, Niccolo E A1 Papandreou, Apostolos A1 Ng, Joanne A1 Barral, Serena A1 Ngoh, Adeline A1 Ben-Pazi, Hilla A1 Willemsen, Michel A A1 Arkadir, David A1 Barnicoat, Angela A1 Bergman, Hagai A1 Bhate, Sanjay A1 Boys, Amber A1 Darin, Niklas A1 Foulds, Nicola A1 Gutowski, Nicholas A1 Hills, Alison A1 Houlden, Henry A1 Hurst, Jane A A1 Israel, Zvi A1 Kaminska, Margaret A1 Limousin, Patricia A1 Lumsden, Daniel A1 McKee, Shane PB Springer Science and Business Media LLC YR 2016 SN 1061-4036 SN 1546-1718 JF Nature Genetics VO 49 IS 2 SP 223 OP 237 LK http://dx.doi.org/https://doi.org/10.1038/ng.3740 DO https://doi.org/10.1038/ng.3740 SF ELIB - SuUB Bremen
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