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Citation of this article
Wen XL, Wang YZ, Zhang XL, Tu JQ, Zhang ZJ, Liu XX, Lu HY, Hao GP, Wang XH, Yang LH, Zhang RJ. Compound heterozygous p.L483P and p.S310G mutations in GBA1 cause type 1 adult Gaucher disease: A case report. World J Clin Cases 2022; 10(36): 13426-13434 [PMID: 36683633 DOI: 10.12998/wjcc.v10.i36.13426]
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Corresponding Author of This Article
Rui-Juan Zhang, MD, Chief Physician, Department of Hematology, The Third Hospital of Shanxi Medical University, The Shanxi Bethune Hospital, The Shanxi Academy of Medical Sciences, The Tongji Shanxi Hospital, The Shanxi Medical University, No. 99 Longcheng Street, Xiaodian District, Taiyuan 030032, Shanxi Province, China. 13593169668@163.com
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Research Domain of This Article
Hematology
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Case Report
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This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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Dec 26, 2022 (publication date) through Jul 23, 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
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