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Sep 16, 2021 (publication date) through Apr 29, 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: | Yang X, Lv ZL, Tang Q, Chen XQ, Huang L, Yang MX, Lan LC, Shan QW. Congenital disorder of glycosylation caused by mutation of ATP6AP1 gene (c.1036G>A) in a Chinese infant: A case report. World J Clin Cases 2021; 9(26): 7876-7885 [PMID: 34621841 DOI: 10.12998/wjcc.v9.i26.7876] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i26/7876.htm |
| Number | Citing Articles |
| 1 |
Hana Alharbi, Earnest James Paul Daniel, Jenny Thies, Irene Chang, Dana L. Goldner, Bobby G. Ng, Peter Witters, Amal Aqul, Frances Velez‐Bartolomei, Gregory M. Enns, Evelyn Hsu, Elizabeth Kichula, Esther Lee, Charles Lourenco, Sheri A. Poskanzer, Sara Rasmussen, Katelyn Saarela, YunZu M. Wang, Kimiyo M. Raymond, Matthew J. Schultz, Hudson H. Freeze, Christina Lam, Andrew C. Edmondson, Miao He. Fractionated plasma N‐glycan profiling of novel cohort of ATP6AP1‐CDG subjects identifies phenotypic association. Journal of Inherited Metabolic Disease 2023; 46(2): 300 doi: 10.1002/jimd.12589
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