Evidence map›Paper›PMID 39064292›Full record

ArticleJournal of clinical medicine2024

Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia.

Ahmad M Almatrafi, Abdulfatah M Alayoubi, Majed Alluqmani, Jamil A Hashmi, Sulman Basit

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Ahmad M AlmatrafiDepartment of Biology, College of Science, Taibah University, Medina 42353, Saudi Arabia.ORCID 0000-0001-9027-5427
Abdulfatah M AlayoubiDepartment of Basic Medical Sciences, College of Medicine, Taibah University, Madinah 42353, Saudi Arabia.ORCID 0000-0001-9250-940X
Majed AlluqmaniDepartment of Neurology, College of Medicine, Taibah University, Medina 42353, Saudi Arabia.ORCID 0000-0002-5416-6247
Jamil A HashmiCenter for Genetics and Inherited Diseases, Taibah University, Madinah 42353, Saudi Arabia.ORCID 0000-0001-8598-8799
Sulman BasitCenter for Genetics and Inherited Diseases, Taibah University, Madinah 42353, Saudi Arabia.ORCID 0000-0003-4294-6825

Funding

The King Salman Center for Disability Research KSRG-2022 -088
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

diagnosing undiagnosedneurodevelopmental disorderspathogenic variantsSLC30A10

Identifiers

PMID39064292
PMCPMC11278008

What OpenQuestion holds

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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.