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遗传性凝血因子Ⅹ缺乏症11例回顾性研究
OBJECTIVE: To analyze the clinical characteristics, laboratory examination, diagnosis, treatment, and outcome of hereditary factor Ⅹ（FⅩ）deficiency. METHODS: Clinical data of 11 patients with congenital FⅩ deficiency were retrospectively analyzed from July 2009 to February 2021. RESULTS: There were 3...
| Formato: | Online Artículo Texto |
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| Lenguaje: | English |
| Publicado: |
Editorial office of Chinese Journal of Hematology
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980670/ https://www.ncbi.nlm.nih.gov/pubmed/35231989 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2022.01.006 |