Evidence map›Paper›PMID 31896839›Full record

ArticleIndian journal of dermatology

Extracellular Matrix Protein 1 Gene Mutation in Turkish Patients with Lipoid Proteinosis.

Selma Bakar Dertlioğlu, Tuba Gökdoğan Edgünlü, Deniz Erol Şen, Tuğba Önal Süzek

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Indian journal of dermatology. 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
0.2field-weighted citation impact, top 39% of its field
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, 3 citations in OpenAlex.

  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

4 authors at 2 institutions in 3 countries.

Selma Bakar DertlioğluDepartment of Dermatology, Dermatology Clinic, Sıtkı Koçman University, Elazığ, Turkey.
Tuba Gökdoğan EdgünlüDepartment of Medical Biology, Sıtkı Koçman University, Elazığ, Turkey.
Deniz Erol ŞenDepartment of Medical Genetics, Fırat Universty, Elazığ, Turkey.
Tuğba Önal SüzekDepartment of Sequence Analysis, Sıtkı Koçman University, Elazığ, Turkey.
Koç University · TRMedical Genetics Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLipoid proteinosis (LP) is a rare autosomal recessive genodermatosis characterized by mucocutaneous lesions and hoarseness of voice that develop in early childhood. LP is caused by mutation in the extracellular matrix protein 1 (

aimsThis study aimed to present the profile of MATERIALS AND

methodsThe

resultsof the 19 LP patients evaluated in our study, we detected defects in exon 6 (c.507delT, 658T>G), exon 9 (157C>T, 727C>T), and exon 10 (c.93_94delGCinsTT) of the

conclusionsOur results indicate that defects in exons 6, 9, and 10 of the

Indexed as

Extracellular matrix protein 1geneticlipoid proteinosismutation

Identifiers

PMID31896839
PMCPMC6862362
OpenAlexW2984183963

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.