Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study-Reference-Cited by-同舟云学术

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

Published:2011-01 Issue:1 Volume:10 Page:54-62
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

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

Publisher

Elsevier BV

Subject

Clinical Neurology

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