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Nov 26, 2022 (publication date) through Jun 16, 2024
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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
| For: | Zhou YQ, Wang XQ, Jiang J, Huang SL, Dai ZJ, Kong QQ. Novel hydroxymethylbilane synthase gene mutation identified and confirmed in a woman with acute intermittent porphyria: A case report. World J Clin Cases 2022; 10(33): 12319-12327 [PMID: 36483813 DOI: 10.12998/wjcc.v10.i33.12319] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i33/12319.htm |
| Number | Citing Articles |
| 1 |
Yi Ren, Shuang Li, Jia-Jia Lei, Ru Li, Bai-Xue Dong, Jing Yang. Clinical feature and genetic analysis of HMBS gene in Chinese patients with acute intermittent porphyria: a systematic review. Frontiers in Genetics 2023; 14 doi: 10.3389/fgene.2023.1291719
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| 2 |
Somarajan Anandan, Sajeesh S Rajendran, Jyothish P Kumar, Divine S Shajee. A rare cause for seizures in an adult male – First report of a rare mutation in HMBS gene (c.730_731del) from India. IP Indian Journal of Neurosciences 2024; 10(1): 51 doi: 10.18231/j.ijn.2024.011
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| 3 |
Xiaoqing Wang, Huifen Zhang, Huanhuan Huang, Wenli Wang, Yuping Wen, Zhuojin Dai, Shuling Huang, Jingyi Zhou, Yuqing Zhou. Functional and structural analysis of a novel splice site HMBS variant in a Chinese AIP patient. Frontiers in Genetics 2023; 14 doi: 10.3389/fgene.2023.1333111
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