Evidence map›Paper›PMID 38974611›Full record

ArticleJIMD reports2024

A founder mutation in

Khalid Al-Thihli, Nadia Al Hashmi, Aaisha Al Balushi, Asila Al-Habsi, Eiman Al-Ajmi, Fatma Al-Jasmi, Fathiya Al-Murshedi

Abstract readCase Reports
In one paragraph

Article in JIMD reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Carbonic anhydrase VA deficiency due to a novelMolecular genetics and metabolism reports · 2025
    Article
  4. A founder mutation inJIMD reports · 2024
    Article
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

7 authors.

Khalid Al-ThihliGenetic & Developmental Medicine Clinic, Department of Genetics Sultan Qaboos University Hospital Muscat Oman.
Nadia Al HashmiDepartment of Pediatrics the Royal Hospital Muscat Oman.
Aaisha Al BalushiDepartment of Pediatrics the Royal Hospital Muscat Oman.
Asila Al-HabsiDepartment of Nursing Sultan Qaboos University Hospital Muscat Oman.
Eiman Al-AjmiDepartment of Radiology and Molecular Imaging Sultan Qaboos University Hospital Muscat Oman.
Fatma Al-JasmiDepartment of Genetics and Genomics, College of Medicine and Health Sciences United Arab Emirates University Al Ain United Arab Emirates.
Fathiya Al-MurshediGenetic & Developmental Medicine Clinic, Department of Genetics Sultan Qaboos University Hospital Muscat Oman.ORCID https://orcid.org/0000-0002-6305-9718

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbonic anhydrase VA (CA-VA) deficiency is a rare cause of hyperammonemia caused by biallelic mutations in

Indexed as

CA5Acarbonic anhydrase‐VACA‐VAfounder mutationhyperammonemiahyperCkemiahypoglycemialactic acidemia

Identifiers

PMID38974611
PMCPMC11224491

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.