Academic Content and Language Evaluation 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 (2494)
All Articles published online
|
Publishing Process of This Article
|
Jan 7, 2022 (publication date) through Jun 17, 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: | Zhao LJ, Zhang ZL, Fu Y. Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families. World J Clin Cases 2022; 10(1): 205-216 [PMID: 35071519 DOI: 10.12998/wjcc.v10.i1.205] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v10/i1/205.htm |
| Number | Citing Articles |
| 1 |
Nandita Sharma, Divya Kumari, Inusha Panigrahi, Preeti Khetarpal. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options. Clinical Genetics 2023; 103(1): 16 doi: 10.1111/cge.14228
|