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Jul 16, 2022 (publication date) through Oct 23, 2025
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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
| Song XL, Peng LY, Wang DW, Wang H. Autosomal dominant osteopetrosis type II resulting from a de novo mutation in the CLCN7 gene: A case report. World J Clin Cases 2022; 10(20): 6936-6943 [PMID: 36051116 DOI: 10.12998/wjcc.v10.i20.6936] |
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| ©2004-2025 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA | |
| For: | Song XL, Peng LY, Wang DW, Wang H. Autosomal dominant osteopetrosis type II resulting from a de novo mutation in the CLCN7 gene: A case report. World J Clin Cases 2022; 10(20): 6936-6943 [PMID: 36051116 DOI: 10.12998/wjcc.v10.i20.6936] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i20/6936.htm |
| Number | Citing Articles |
| 1 |
Mengxiao Liu, Hao Zheng, Zhixiang Li, Runfei Pang, Yang Niu, Lei Yang, Zhenxiang Zhang, Jianguo Xia, Xiuhong Pang. A novel frameshift variant leads to familial osteopetrosis with variable phenotypes in a Chinese Han consanguineous family. BMC Medical Genomics 2025; 18(1) doi: 10.1186/s12920-025-02101-y
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| 2 |
Jelena M. Živković, Jelena G. Najdanović, Stevo J. Najman. Mutations in Osteoclast Genes as Causes of Osteoclast-Related Diseases. DNA and Cell Biology 2025; doi: 10.1177/10445498251368298
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