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Jan 21, 2022 (publication date) through Jul 22, 2025
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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: | Wu WJ, Sun SZ, Li BG. Congenital muscular dystrophy caused by beta1,3-N-acetylgalactosaminyltransferase 2 gene mutation: Two case reports. World J Clin Cases 2022; 10(3): 1056-1066 [PMID: 35127920 DOI: 10.12998/wjcc.v10.i3.1056] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i3/1056.htm |
| Number | Citing Articles |
| 1 |
Xiaona Fu, Hui Wang, Wenjia Chai, Xiaoyu Chen, Danyu Song, Wei Wang, Jingwei Zhong, Zhimei Liu, Xiao Tong, Hui Xiong, Xiaotun Ren, Jingang Gui.
Pathogenic mechanisms and clinical insights into
B3GALNT2
-related alpha-dystroglycanopathies
. Journal of Neuromuscular Diseases 2025; doi: 10.1177/22143602251360270
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| 2 |
M.A. Cubilla, G.M. Papazoglu, C.G. Asteggiano. Dystroglycanopathies: Genetic Bases of Muscular Dystrophies Due to Alteration in the O-Glycosylation of α-Dystroglycan. Journal of Inborn Errors of Metabolism and Screening 2023; 11 doi: 10.1590/2326-4594-jiems-2022-0005
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