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May 26, 2022 (publication date) through Nov 25, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Fu P, Jiao YY, Chen K, Shao JB, Liao XL, Yang JW, Jiang SY. Targeted next-generation sequencing identifies a novel nonsense mutation in ANK1 for hereditary spherocytosis: A case report. World J Clin Cases 2022; 10(15): 4923-4928 [PMID: 35801015 DOI: 10.12998/wjcc.v10.i15.4923] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i15/4923.htm |
| Number | Citing Articles |
| 1 |
Linlin Xu, Xiaofeng Wei, Guanxia Liang, Dina Zhu, Yanxia Zhang, Yang Zhang, Xuan Shang. A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2023; 1869(1): 166595 doi: 10.1016/j.bbadis.2022.166595
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| 2 |
Çağrı Coşkun. Clinical and genetic diagnosis of two Turkish patients with hereditary spherocytosis. The European Research Journal 2024; : 1 doi: 10.18621/eurj.1512399
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| 3 |
Meiyun Kang, Huimin Li, Jun Zhu, Liwen Zhu, Yue Hong, Yongjun Fang. Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis. Frontiers in Genetics 2023; 14 doi: 10.3389/fgene.2023.1088985
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