Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

Autor: 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 EA, Maher, Eamonn R

Publikováno v: In The Lancet Neurology January 2011 10(1):54-62

Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist

Autor: Blackstone, Craig¹ blackstc@ninds.nih.gov, Kurian, Manju A² (AUTHOR), Li, Yan (AUTHOR), Zhen, Juan (AUTHOR), Meyer, Esther (AUTHOR), Hai, Nebula (AUTHOR), Christen, Hans-Jürgen (AUTHOR), Hoffmann, Georg F (AUTHOR), Jardine, Philip (AUTHOR), von Moers, Arpad (AUTHOR), Mordekar, Santosh R (AUTHOR), O'Callaghan, Finbar (AUTHOR), Wassmer, Evangeline (AUTHOR), Wraige, Elizabeth (AUTHOR), Dietrich, Christa (AUTHOR), Lewis, Timothy (AUTHOR), Hyland, Keith (AUTHOR), Heales, Simon Jr (AUTHOR), Sanger, Terence (AUTHOR), Gissen, Paul (AUTHOR)

Publikováno v: Lancet Neurology. Jan2011, Vol. 10 Issue 1, p24-25. 2p.