ArticleArchives of Iranian medicine2024
A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in
Farzane Zare Ashrafi, Saeed Dorgaleleh, Raziye Rezvani Rezvandeh, Negar Kazemi, Nasrin Azizi, Masoud Edizadeh, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi, Reza Najafipour and 1 more
Abstract read
In one paragraphArticle in Archives of Iranian medicine, 2024. 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
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
11 authors.
Farzane Zare AshrafiGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.ORCID 0000-0002-8163-5221 Saeed DorgalelehGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Raziye Rezvani RezvandehGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Negar KazemiGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Nasrin AziziGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Masoud EdizadehDepartment of Bioinformatics, Genoks Genetic Diagnosis Center, Ankara, Turkey.
Mohammad Hossein AziziAcademy of Medical Sciences of IR Iran, Tehran, Iran.
Kimia KahriziGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Hossein NajmabadiGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Reza NajafipourGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Marzieh MohseniGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.ORCID 0000-0003-1200-4044 Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
Indexed as
Connexin 26Sulfate TransportersAdolescentAdultChildChild, PreschoolExome SequencingFemaleFounder EffectHearing Loss, SensorineuralHumansIranMaleMembrane Transport ProteinsMutation, MissensePedigreeConnexin 26GJB2 protein, humanMembrane Transport ProteinsSLC26A4 protein, humanSulfate TransportersExome sequencingFounder mutationIranNon-syndromic hearing lossSLC26A4
Identifiers
PMID39465527
PMCPMC11496598
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