Article
Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Apr 2016
Dorgalaleh Akbar, Zaker Farhad, Tabibian Shadi, Alizadeh Shaban, Dorgalele Saeed, Hosseini Soudabeh, Shamsizadeh Morteza
Abstract excerpt
Congenital factor X deficiency is one of the most severe forms of rare bleeding disorders transmitted in autosomal recessive manner. According to the World Federation of Hemophilia survey, 153 patients with factor X deficiency (FXD) live in Iran, but a few studies have been performed to determine the precise distribution of FXD in different parts of the country and to assess molecular basis of this disorder in...
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