Evidence map›Paper›PMID 32957425›Full record

ReviewInternational journal of molecular sciences2020

Mucolipidoses Overview: Past, Present, and Future.

Shaukat A Khan, Saori C Tomatsu

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Cellular Lyso-Gb3 Is a Biomarker for Mucolipidosis II.International journal of molecular sciences · 2025
    Article
  9. Article
  10. Novel Phenotypical and Biochemical Findings in Mucolipidosis Type II.International journal of molecular sciences · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Golgi defect as a major contributor to lysosomal dysfunction.Frontiers in cell and developmental biology · 2024
    Review
  18. Review
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

Shaukat A KhanNemours/Alfred I. duPont Hospital for Children, Wilmington, DE 19803, USA.
Saori C TomatsuDepartment of Biological Sciences, University of Delaware, Newark, DE 19716, USA.ORCID 0000-0002-8244-3571
Alfred I. duPont Hospital for Children · USUniversity of Delaware · US

Funding

Center for Biomedical Research Excellence P30GM114736
6 · The paper itself

Abstract

Mucolipidosis II and III (ML II/III) are caused by a deficiency of uridine-diphosphate

Indexed as

AnimalsBiological Transport, ActiveDisease Models, AnimalEnzyme Replacement TherapyGenetic TherapyGlycosaminoglycansHematopoietic Stem Cell TransplantationHumansLysosomesMannosephosphatesMucolipidosesGlycosaminoglycansmannose-6-phosphateMannosephosphatesglycosaminoglycansI-cell diseaseinclusion bodylysosomal storage disorderslysosome enzyme transportmannose 6-phosphate

Identifiers

PMID32957425
PMCPMC7555117
OpenAlexW3086559968

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.