Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
遗传性多巴胺转运体缺乏综合征的临床和分子特征:一项观察性队列研究和实验研究
期刊:Lancet Neurology
影响因子:45.5
doi:10.1016/S1474-4422(10)70269-6
Kurian, Manju A; Li, Yan; Zhen, Juan; Meyer, Esther; Hai, Nebula; Christen, Hans-Jürgen; Hoffmann, Georg F; Jardine, Philip; von Moers, Arpad; Mordekar, Santosh R; O'Callaghan, Finbar; Wassmer, Evangeline; Wraige, Elizabeth; Dietrich, Christa; Lewis, Timothy; Hyland, Keith; Heales, Simon Jr; Sanger, Terence; Gissen, Paul; Assmann, Birgit E; Reith, Maarten E A; Maher, Eamonn R