Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region.
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DOI: 10.1080/16078454.2021.1893977
Abstract: BACKGROUND : Congenital dysfibrinogenemia (CD) is a coagulation disorder caused by mutations in the fibrinogen genes, which result in abnormal fibrinogen function. However, the precise pathogenesis underlying it remains unclear. METHODS : In this study,… read more here.
Keywords: fibrinogen; caused ala327val; congenital dysfibrinogenemia; ala327val mutation ... See more keywords