Erratum: "That DAT" gene that causes dystonia-parkinsonism: broadening the phenotype (Brain 2014) 137 (976-77) Doi:10.1093/brain/awu056);'That DAT' gene that causes dystonia-parkinsonism: Broadening the phenotype

Brain

Volumn 137, Issue 4, 2014, Pages 976-977

  Bhatia, Kailash P ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE TRANSPORTER; PARKIN; SLC6A3 PROTEIN, HUMAN;

COHORT ANALYSIS; DISEASE COURSE; DYSTONIA; GENE; GENE MUTATION; HETEROLOGOUS EXPRESSION; HUMAN; NOTE; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL; TREMOR; DEFICIENCY; FEMALE; GENETIC ASSOCIATION; GENETICS; MALE; MOTOR DYSFUNCTION;

DOPAMINE PLASMA MEMBRANE TRANSPORT PROTEINS; FEMALE; GENETIC ASSOCIATION STUDIES; HUMANS; MALE; MOVEMENT DISORDERS;

EID: 84897831355     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awu170     Document Type: Erratum

References (6)

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2. Kurian MA, Li Y, Zhen J, Meyer E, Hai N, Christen HJ, et al. Clinical and molecular characterisation of hereditary Dopamine Transporter deficiency syndrome: an observational cohort and experimental study. Lancet Neurol 2011; 10: 54-62.
3. Henriksen FH, Yasmeen S, Skjorringe T, Arends NV, Karlsborg M, Hjermind LE, et al. Atypicaldopamine transporter deficiency syndrome in two adult males with molecular characterisation of new transporter variants. Society of Neuroscience Meeting Planner 2012; Poster 042.
4. Ng J, Zhen J, Meyer E, Erreger K, Li Y, Kakar N, et al. Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood. Brain 2014; 137: 1107-19.
5. Schneider SA, Bhatia KP. Rare causes of dystonia parkinsonism [Review]. Curr Neurol Neurosci Rep 2010; 10: 431-9.
6. Torres GE, Gainetdinov RR, Caron MG. Plasma membrane monoamine transporters: structure, regulation and function [Review]. Nat Rev Neurosci 2003; 4: 13-25.