Evidence map›Paper›PMID 39858623›Full record

ArticleGenes2025

Compound Heterozygous p.(R124C) (Classic Lattice Corneal Dystrophy) and p.(R124H) (Granular Corneal Dystrophy Type 2) in

Ji Sang Min, Tae-Im Kim, Ikhyun Jun, R Doyle Stulting, Changrae Rho, Sang Beom Han, Heeyoung Kim, Jinseok Choi, Jinu Han, Eung Kweon Kim

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 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

10 authors.

Ji Sang MinThe Cornea Dystrophy Research Institute, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemungu, Seoul 03722, Republic of Korea.
Tae-Im KimThe Cornea Dystrophy Research Institute, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemungu, Seoul 03722, Republic of Korea.ORCID 0000-0001-6414-3842
Ikhyun JunThe Cornea Dystrophy Research Institute, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemungu, Seoul 03722, Republic of Korea.ORCID 0000-0002-2160-1679
R Doyle StultingWoolfson Eye Institute, Atlanta, GA 30328, USA.ORCID 0000-0003-3635-1913
Changrae RhoSaevit Eye Hospital, Goyang-si 10447, Republic of Korea.
Sang Beom HanSaevit Eye Hospital, Goyang-si 10447, Republic of Korea.ORCID 0000-0003-4757-1575
Heeyoung KimSaevit Eye Hospital, Goyang-si 10447, Republic of Korea.
Jinseok ChoiSaevit Eye Hospital, Goyang-si 10447, Republic of Korea.
Jinu HanInstitute of Vision Research, Department of Ophthalmology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul 06273, Republic of Korea.ORCID 0000-0002-8607-6625
Eung Kweon KimThe Cornea Dystrophy Research Institute, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemungu, Seoul 03722, Republic of Korea.ORCID 0000-0002-1453-8042

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: The phenotypes of classic lattice corneal dystrophy (LCD) and granular corneal dystrophy type 2 (GCD2) that result from abnormalities in

Indexed as

Corneal Dystrophies, HereditaryExtracellular Matrix ProteinsTransforming Growth Factor betaAdultbetaIG-H3 ProteinGenotypeHeterozygoteHumansMalePedigreePhenotypePhotorefractive KeratectomybetaIG-H3 ProteinExtracellular Matrix ProteinsTransforming Growth Factor betaclassic lattice corneal dystrophy (LCD)compound mutation of TGFBIgranular corneal dystrophy type 2 (GCD2)TA cloning

Identifiers

PMID39858623
PMCPMC11765409

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.