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

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

author	[Person:5660691] Kurian, MA [Person:1614736] Li, Y [Person:5660720] Zhen, J [Person:5660727] Meyer, E [Person:5660707] Hai, N [Person:5660728] Christen, HJ [Person:200236] Hoffmann, GF [Person:5660711] Jardine, P [Person:5660690] von Moers, A [Person:5660697] Mordekar, SR [Person:5660708] O'Callaghan, F [Person:5660726] Wassmer, E [Person:5660714] Wraige, E [Person:5660687] Dietrich, C [Person:5660685] Lewis, T [Person:71117] Hyland, K [Person:5660698] Heales, S [Person:5660709] Sanger, T [Person:5628811] Gissen, P [Person:5660695] Assmann, BE [Person:5660713] Reith, ME [Person:2471669] Maher, ER
created	[InstanceEdit:5660699] Jassal, Bijay, 2015-01-06
dbId	5660704
displayName	Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
journal	Lancet Neurol
pages	54-62
pubMedIdentifier	21112253
schemaClass	LiteratureReference
title	Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
url	http://www.ncbi.nlm.nih.gov/pubmed/21112253
volume	10
year	2011

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[FailedReaction:R-HSA-5660706] Defective SLC6A3 does not cotransport DA, Na+ from extracellular region to cytosol

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