Evidence map›Paper›PMID 27780564›Full record

ArticleMolecular genetics and metabolism2016

Corrigendum to "GJC2 promoter mutations causing Pelizaeus-Merzbacher-like disease" [Mol. Genet. Metab. 111 (2014) 393-398].

Leo Gotoh, Ken Inoue, Guy Helman, Sara Mora, Kiran Maski, Janet S Soul, Miriam Bloom, Sarah H Evans, Yu-Ichi Goto, Ljubica Caldovic and 2 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Molecular genetics and metabolism, 2016. 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

5 · Who and what money

Authors and funding

12 authors.

Leo GotohDepartment of Mental Retardation and Birth Defects Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Ken InoueDepartment of Mental Retardation and Birth Defects Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Guy HelmanDepartment of Neurology, Children's National Medical Center, Washington, DC, USA.
Sara MoraNemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, DE, USA.
Kiran MaskiDepartment of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Janet S SoulDepartment of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Miriam BloomDepartment of Pediatrics, Children's National Medical Center, Washington, DC, USA.
Sarah H EvansDepartment of Physical Medicine and Rehabilitation, Children's National Medical Center, Washington, DC, USA.
Yu-Ichi GotoDepartment of Mental Retardation and Birth Defects Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Ljubica CaldovicCenter for Genetic Medicine Research, Children's National Medical Center, Washington, DC, USA.
Grace M HobsonNemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, DE, USA; Center for Genetic Medicine Research, Children's National Medical Center, Washington, DC, USA; Department of Biological Sciences, University of Delaware, Newark, DE, USA.
Adeline VanderverDepartment of Neurology, Children's National Medical Center, Washington, DC, USA; Department of Pediatrics, Children's National Medical Center, Washington, DC, USA; Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA, USA. Electronic address: avanderv@childrensnational.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID27780564

What OpenQuestion holds

Textmetadata
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.