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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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2021
Materias:
论著
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120128/
https://www.ncbi.nlm.nih.gov/pubmed/33979974
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.04.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120128/
https://www.ncbi.nlm.nih.gov/pubmed/33979974
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.04.006

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