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遗传性凝血因子Ⅴ缺乏症九例基因分析
OBJECTIVE: To analyze the clinical phenotype and molecular pathogenesis of nine patients with hereditary factor Ⅴ（FⅤ）deficiency. METHODS: Nine patients with hereditary FⅤ deficiency who were admitted to the Institute of Hematology and Blood Diseases Hospital from April 1999 to September 2019 were an...
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| Publicado no: | Zhonghua Xue Ye Xue Za Zhi |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Editorial office of Chinese Journal of Hematology
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8120128/ https://ncbi.nlm.nih.gov/pubmed/33979974 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.04.006 |
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