Evidence map›Paper›PMID 39995829›Full record

ArticleFrontiers in medicine2024

Case report: A novel 11-bp deletion in exon 11 causing a frameshift in the C-terminal of the

Salam Al Kindi, Altaf Al-Mamari, Shoaib Al-Zadjali, Mohamed Al-Rawahi, Ali Al Madhani, Anil V Pathare

Abstract readCase Reports
In one paragraph

Article in Frontiers in 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

6 authors.

Salam Al KindiDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, Oman.
Altaf Al-MamariDepartment of Medicine, Sohar Hospital, Sohar, Oman.
Shoaib Al-ZadjaliDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, Oman.
Mohamed Al-RawahiDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, Oman.
Ali Al MadhaniDepartment of Medicine, Sohar Hospital, Sohar, Oman.
Anil V PathareDepartment of Haematology, Sultan Qaboos University Hospital, Muscat, Oman.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked sideroblastic anemia (XLSA) (MIM 300752) is the most common genetic form of sideroblastic anemia, a heterogeneous group of disorders characterized by iron deposits in the mitochondria of erythroid precursors. It is due to mutations of the erythroid-specific enzyme

Indexed as

ALAS2congenitalsideroblastic anemiaX-linkedXLSA

Identifiers

PMID39995829
PMCPMC11847639

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.