Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (3266)
All Articles published online
|
Publishing Process of This Article
|
Aug 26, 2022 (publication date) through Dec 25, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Wu XH, Lin SZ, Zhou YQ, Wang WQ, Li JY, Chen QD. VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report. World J Clin Cases 2022; 10(24): 8749-8754 [PMID: 36157797 DOI: 10.12998/wjcc.v10.i24.8749] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v10/i24/8749.htm |
| Number | Citing Articles |
| 1 |
Christina Del Greco, Anthony Antonellis. The Role of Nuclear-Encoded Mitochondrial tRNA Charging Enzymes in Human Inherited Disease. Genes 2022; 13(12): 2319 doi: 10.3390/genes13122319
|
| 2 |
Shannon Strader, Marissa Vawter‐Lee, Loren Pena, Heather Huxol, Corrie Harris. Why genetic testing is important in patients with developmental disabilities—a unique case of progressive hypertonia and chorea: VARS2‐related disorder. PM&R 2024; doi: 10.1002/pmrj.13267
|