Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A.
作者信息
Vilar Rui, Casini Alessandro, Fournel Alexandra, Mourey Guillaume, Neerman-Arbez Marguerite
机构信息
Department of Genetic Medicine and Development, University of Geneva Faculty of Medicine, Switzerland.
Division of Angiology and Hemostasis, University Hospitals, University of Geneva Faculty of Medicine, Switzerland.
出版信息
Thromb Res. 2020 Sep;193:5-8. doi: 10.1016/j.thromres.2020.05.040. Epub 2020 May 28.
Abstract
摘要
Zotero 插件