Cargando…
不同家系遗传性蛋白C缺陷症12例临床表型和基因突变分析
OBJECTIVE: To investigate the molecular pathogenesis and clinical features of unrelated 12 patients with inherited coagulation protein C(PC)deficiency in Chinese population. METHODS: The PC activity(PC:A)and PC antigen(PC:Ag)were detected by chromogenic substrate and enzyme linked immunosorbent assa...
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Editorial office of Chinese Journal of Hematology
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980666/ https://www.ncbi.nlm.nih.gov/pubmed/35231991 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2022.01.008 |
Ejemplares similares
-
一个遗传性抗凝血酶缺陷症家系的表型与基因突变分析
Publicado: (2020) -
一个遗传性凝血因子Ⅶ缺陷症家系的临床特征和基因分析
Publicado: (2015) -
一个遗传性凝血因子Ⅻ缺乏症家系的临床表型及基因分析
Publicado: (2018) -
一个遗传性凝血因子Ⅺ缺陷症家系基因分析
Publicado: (2020) -
一个遗传性凝血因子XIII缺陷症家系的基因诊断
Publicado: (2015)