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 (5896)
All Articles published online
|
Featured Article
|
Publishing Process of This Article
|
Sep 6, 2020 (publication date) through May 8, 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: | Hu XM, Yuan K, Chen H, Chen C, Fang YL, Zhu JF, Liang L, Wang CL. Novel deletion mutation in Bruton’s tyrosine kinase results in X-linked agammaglobulinemia: A case report. World J Clin Cases 2020; 8(17): 3859-3866 [PMID: 32953865 DOI: 10.12998/wjcc.v8.i17.3859] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v8/i17/3859.htm |
| Number | Citing Articles |
| 1 |
Lin Zhang, Su Li Zhao, Zhi Hong Wang. Diverse clinical manifestations of X-linked adrenoleukodystrophy in a Chinese family with identical multisite variants of ABCD1 gene. Psychiatric Genetics 2021; 31(5): 162 doi: 10.1097/YPG.0000000000000292
|