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146例先天性纤维蛋白原病的基因突变谱及纤维蛋白原输注药代动力学分析
OBJECTIVE: To investigate the clinical type and gene mutations, clinical manifestations, laboratory tests, diagnosis, and fibrinogen replacement therapy of congenital fibrinogen disorders. METHODS: Clinical data of 146 patients with congenital fibrinogen disorders diagnosed from April 2000 to Novemb...
| Formato: | Online Artículo Texto |
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| Lenguaje: | English |
| Publicado: |
Editorial office of Chinese Journal of Hematology
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408493/ https://www.ncbi.nlm.nih.gov/pubmed/34455742 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.07.005 |