Evidence map›Paper›PMID 37443770›Full record

ReviewCells2023

Dopamine Transporter Deficiency Syndrome (DTDS): Expanding the Clinical Phenotype and Precision Medicine Approaches.

Joanne Ng, Serena Barral, Simon N Waddington, Manju A Kurian

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Genotype-Phenotype Relations for the Dystonia-Parkinsonism GenesInternational journal of molecular sciences · 2025
    Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Joanne NgGene Transfer Technology Group, EGA UCL Institute for Women's Health, University College London, London WC1E 6HX, UK.ORCID 0000-0002-7946-9965
Serena BarralDevelopmental Neurosciences, Zayed Centre for Research into Rare Disease in Children, GOS UCL Institute of Child Health, University College London, London WC1N 1DZ, UK.ORCID 0000-0002-1430-3614
Simon N WaddingtonGene Transfer Technology Group, EGA UCL Institute for Women's Health, University College London, London WC1E 6HX, UK.ORCID 0000-0003-4970-4730
Manju A KurianDevelopmental Neurosciences, Zayed Centre for Research into Rare Disease in Children, GOS UCL Institute of Child Health, University College London, London WC1N 1DZ, UK.
University College London · GBGreat Ormond Street Hospital · GBSouth African Medical Research Council · ZA

Funding

Medical Research Council MR/K02342X/1Medical Research Council MR/R015325/1Medical Research Council MR/T016809/1Wellcome TrustWellcome Trust WT098524MA
6 · The paper itself

Abstract

Infantile parkinsonism-dystonia due to dopamine transporter deficiency syndrome (DTDS) is an ultrarare childhood movement disorder caused by biallelic loss-of-function mutations in the

Indexed as

Dopamine Plasma Membrane Transport ProteinsPrecision MedicineDystonic DisordersParkinson DiseasePhenotypeThymidineTriphenylmethyl Compounds5'-O-(4,4'-dimethoxytrityl)thymidine-3'-O-(2,4-dinitrophenyl) succinateDopamine Plasma Membrane Transport ProteinsThymidineTriphenylmethyl CompoundsDATdopamine transporter deficiency syndromegene therapyinfantile parkinsonism-dystoniaiPSCneurotransmitterSLC6A3

Identifiers

PMID37443770
PMCPMC10341083
OpenAlexW4382722109

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.