Evidence map›Paper›PMID 30298423›Full record

ArticleActa neurologica Belgica2019

A new NBIA patient from Turkey with homozygous C19ORF12 mutation.

Çiğdem Seher Kasapkara, Leyla Tümer, Allison Gregory, Fatih Ezgü, Aslı İnci, Betül Emine Derinkuyu, Rachel Fox, Caleb Rogers, Susan Hayflick

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

Article in Acta neurologica Belgica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Case Report: Identification of aFrontiers in genetics · 2022
    Article
  3. Review
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

9 authors.

Çiğdem Seher KasapkaraDepartment of Pediatric Metabolism and Nutrition, Dr. Sami Ulus Maternity and Children's Research and Education Hospital, Ankara, Turkey. cskasapkara@gmail.com.
Leyla TümerDepartment of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
Allison GregoryMolecular and Medical Genetics, Pediatrics and Neurology, Oregon Health and Science University, Portland, Oregon, 97239, USA.
Fatih EzgüDepartment of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
Aslı İnciDepartment of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
Betül Emine DerinkuyuDepartment of Pediatric Radiology, Dr. Sami Ulus Maternity and Children's Research and Education Hospital, Ankara, Turkey.
Rachel FoxMolecular and Medical Genetics, Pediatrics and Neurology, Oregon Health and Science University, Portland, Oregon, 97239, USA.
Caleb RogersMolecular and Medical Genetics, Pediatrics and Neurology, Oregon Health and Science University, Portland, Oregon, 97239, USA.
Susan HayflickMolecular and Medical Genetics, Pediatrics and Neurology, Oregon Health and Science University, Portland, Oregon, 97239, USA.

Funding

UW Center for Mendelian GenomicsUM1HG006493 · NHGRI · UNIVERSITY OF WASHINGTON · PI BAMSHAD, MICHAEL JOSEPH, LEAL, SUZANNE M · 2016 to 2020
$15.3M
NHGRI NIH HHS 2UM1HG006493NHGRI NIH HHS UM1 HG006493
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HomozygoteHumansIron Metabolism DisordersMitochondrial ProteinsMutationNeuroaxonal DystrophiesTurkeyC19orf12 protein, humanMitochondrial Proteins

Identifiers

PMID30298423
PMCPMC7556727

What OpenQuestion holds

Textmetadata
LicenceTDM
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.