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Jan 21, 2022 (publication date) through Jun 3, 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: | 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 |
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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