Clinical features of fructose-1,6-bisphosphatase deficiency in 4 children and literature review
Objective To summarize the clinical features and genetic variation characteristics of children with fructose-1,6-bisphosphatase deficiency (FBP1D) caused by FBP1 gene variations. Methods Four pediatric patients with FBP1D admitted from January 2019 to June 2025 were enrolled as study subjects. Their...
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| Formatua: | Artigo |
| Hizkuntza: | Chinês |
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Editorial Office of Journal of Clinical Pediatrics
2026-05-01
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| Saila: | Linchuang erke zazhi |
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| Sarrera elektronikoa: | https://jcp.xinhuamed.com.cn/fileup/1000-3606/PDF/1778223611591-1422129414.pdf |
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