Evidence map›Paper›PMID 31497560›Full record

ArticleIranian journal of public health2019

First Report of a Known Pathogenic Variant in the

Mirsajjad Mousavi-Asl Germeh Cheshmeh, Ali Najizadeh, Saied Hosseini-Asl, Hooshang Zaimkohan, Roshanak Jazayeri

Abstract readCase Reports
In one paragraph

Article in Iranian journal of public health, 2019. 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

5 authors.

Mirsajjad Mousavi-Asl Germeh CheshmehStudent Research Committee, Ardabil University of Medical Sciences, Ardabil, Iran.
Ali NajizadehStudent Research Committee, Alborz University of Medical Sciences, Karaj, Iran.
Saied Hosseini-AslHoma Gene Clinic, Department of Genetics, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
Hooshang ZaimkohanNon-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Roshanak JazayeriNon-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital Nail abnormalities are rare ectodermal defects. Autosomal recessive nail dysplasia is much rarer. Recently it has been recognized as a condition resulting in nail dystrophy in the absence of other cutaneous or extracutaneous disorders. Few case reports have identified mutations in the Frizzled 6 (

Indexed as

Autosomal recessiveFZD6 geneIranNail dysplasia

Identifiers

PMID31497560
PMCPMC6708523

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.