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2019
Dafsari, Hormos Salimi, Sprute, Rosanne 
ORCID: 0000-0003-2457-6437, Wunderlich, Gilbert, Daimagueler, Huelya-Sevcan, Karaca, Ezgi ORCID: 0000-0002-4926-7991, Contreras, Adriana, Becker, Kerstin, Schulze-Rhonhof, Mira, Kiening, Karl, Karakulak, Tulay ORCID: 0000-0002-4644-2774, Kloss, Manja, Horn, Annette, Pauls, Amande, Nuernberg, Peter, Altmueller, Janine, Thiele, Holger, Assmann, Birgit, Koy, Anne and Cirak, Sebahattin
(2019).
Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia.
J. Hum. Genet., 64 (8).
S. 803 - 814.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 1435-232X