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Jan 26, 2021 (publication date) through Feb 2, 2025
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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: | Cao LX, Liu Y, Song ZJ, Zhang BR, Long WY, Zhao GH. Compound heterozygous mutations in the neuraminidase 1 gene in type 1 sialidosis: A case report and review of literature. World J Clin Cases 2021; 9(3): 623-631 [PMID: 33553400 DOI: 10.12998/wjcc.v9.i3.623] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i3/623.htm |
| Number | Citing Articles |
| 1 |
Yuan Ding, Ming Cheng, Chunxiu Gong. Two cases of type I sialidosis and a literature review. Orphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03431-3
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| 2 |
Mei-Ling Peng, Siu-Fung Chau, Jia-Ying Chien, Peng-Yeong Woon, Yu-Chen Chen, Wai-Man Cheang, Hsien-Yang Tsai, Shun-Ping Huang. Genetic Insights and Clinical Implications of NEU1 Mutations in Sialidosis. Genes 2025; 16(2): 151 doi: 10.3390/genes16020151
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| 3 |
Mustafa Kılıç, Suzan İcil, Abdullah Sezer, Öznur Kaya-Güneş, Selim S. Comoğlu. Sialidosis type 1 in a Turkish family: a case report and review of literatures. Journal of Pediatric Endocrinology and Metabolism 2024; doi: 10.1515/jpem-2024-0468
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