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Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia

Title:	Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia
Authors:	Dafsari, Hormos Salimi^{Aff1, Aff2}; Sprute, Rosanne^{Aff1, Aff2}; Wunderlich, Gilbert^{Aff3, Aff4}; Daimagüler, Hülya-Sevcan^{Aff1, Aff2}; Karaca, Ezgi^{Aff5, Aff6}; Contreras, Adriana^{Aff1, Aff2}; Becker, Kerstin^{Aff1, Aff2}; Schulze-Rhonhof, Mira^Aff1; Kiening, Karl^Aff7; Karakulak, Tülay^{Aff5, Aff6}; Kloss, Manja^Aff8; Horn, Annette^Aff9; Pauls, Amande^Aff4; Nürnberg, Peter^Aff10; Altmüller, Janine^Aff10; Thiele, Holger^Aff10; Assmann, Birgit^Aff11; Koy, Anne^{Aff1, Aff3}; Cirak, Sebahattin^{Aff1, Aff2, Aff3, cor19}
Source:	Journal of Human Genetics. 64(10):1051-1054
Database:	Springer Nature Journals