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...

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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/PMC8408493/
https://www.ncbi.nlm.nih.gov/pubmed/34455742
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.07.005

Internet

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

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