Evidence map›Paper›PMID 33552644›Full record

ArticleJournal of pediatric genetics2021

Genotype to Phenotype: Identification of Mucopolysaccharidosis Type IIIB (Sanfilippo's B) Case Using Whole Exome Sequencing.

Muhsin Elmas, Basak Gogus, Furkan Kılıçarslan, Aysegul Bukulmez, Mustafa Solak

Open access · greenAbstract readCase Reports
In one paragraph

Article in Journal of pediatric genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Muhsin ElmasMedical Genetics Department, Afyonkarahisar Health Sciences University, Afyonkarahisar, Turkey.ORCID 0000-0002-5626-2160
Basak GogusMedical Genetics Department, Afyonkarahisar Health Sciences University, Afyonkarahisar, Turkey.
Furkan KılıçarslanFaculty of Arts and Sciences, Genetics & Bioinformatics, Bahcesehir University, Istanbul, Turkey.ORCID 0000-0002-4403-2835
Aysegul BukulmezPediatry Department, Afyonkarahisar Health Sciences University, Afyonkarahisar, Turkey.ORCID 0000-0002-6013-5172
Mustafa SolakMedical Genetics Department, Afyonkarahisar Health Sciences University, Afyonkarahisar, Turkey.ORCID 0000-0001-5348-9645
Afyonkarahisar Sağlık Bilimleri ÜniversitesiBahçeşehir University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucopolysaccharidosis type IIIB (Sanfilippo's B; OMIM no.: 252920) is a lysosomal storage disorder caused by defective degradation of heparan sulfate. The enzyme that has decreased function in this disease is α-N acetylglucosaminidase. This enzyme is encoded by the

Indexed as

consanguineous marriagemucopolysaccharidosis IIISanfilippo's syndrome Bwhole exome sequencing

Identifiers

PMID33552644
PMCPMC7853908
OpenAlexW3015118605

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.