دورية أكاديمية

Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only

التفاصيل البيبلوغرافية
العنوان: Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only
المؤلفون: Wilcox, Robert, Brænne, Ingrid, Brüggemann, Norbert, Winkler, Susen, Wiegers, Karin, Bertram, Lars, Anderson, Tim, Lohmann, Katja
المصدر: Journal of Neurology: Official Journal of the European Neurological Society. January 2015 262(1):187-193
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:03405354
14321459
DOI:10.1007/s00415-014-7547-9