Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only
Crossref DOI link: https://doi.org/10.1007/s00415-014-7547-9
Published Online: 2014-10-31
Published Print: 2015-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Wilcox, Robert
Brænne, Ingrid
Brüggemann, Norbert
Winkler, Susen
Wiegers, Karin
Bertram, Lars
Anderson, Tim
Lohmann, Katja
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