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

Manju A. Kurian^*, Yan Li, Juan Zhen, Esther Meyer, Nebula Hai, Hans-Juergen Christen, Georg F. Hoffmann, Philip Jardine, Arpad von Moers, Santosh R. Mordekar, Finbar O'Callaghan, Evangeline Wassmer, Elizabeth Wraige, Christa Dietrich, Timothy Lewis, Keith Hyland, Simon J. R. Heales, Terence Sanger, Paul Gissen, Birgit E. AssmannMaarten E. A. Reith, Eamonn R. Maher

^*Corresponding author for this work

University of Birmingham
Birmingham Children's Hospital NHS Trust
Birmingham Women's NHS Foundation Trust
New York University
Childrens Hosp Bult
Heidelberg University
Bristol Childrens Hosp, Dept Paediat Neurol
Childrens Hosp, Kliniken Berlin Westend
Sheffield Children's Hospital
Frenchay Hosp, Dept Radiol
University of Bristol
Natl Hosp, Neurometab Unit
Great Ormond St Hosp Sick Children, University College London, University of London
USC University of Southern California
Univ Childrens Hosp, Dept Gen Paediat

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

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