Evidence map›Paper›PMID 41306488›Full record

ReviewMolecular vision2025

Bietti crystalline corneoretinal dystrophy: Advances in understanding and gene therapeutic approaches.

Guangrong Zhao, Dayou Ding

Abstract readReview
In one paragraph

Review in Molecular vision, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Guangrong ZhaoSchool of Chemical Engineering and Technology, Tianjin University, Tianjin, P. R. China.
Dayou DingSchool of Chemical Engineering and Technology, Tianjin University, Tianjin, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bietti crystalline dystrophy (BCD), an autosomal recessive inherited retinal disorder caused by mutations in the

Indexed as

Corneal Dystrophies, HereditaryGenetic TherapyRetinal DiseasesAnimalsCytochrome P-450 Enzyme SystemCytochrome P450 Family 4DependovirusHumansMutationCYP4V2 protein, humanCytochrome P-450 Enzyme SystemCytochrome P450 Family 4

Identifiers

PMID41306488
PMCPMC12645063

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.