Role of Pro564Leu of FXIII-A Gene Polymorphism and Risk of Central Nervous Bleeding in Patients with Congenital Factor XIII Deficiency, Southeast of Iran

Background: The deficiency of factor XIII is a rare hemorrhagic disorder with the highest global incidence in Sistan and Baluchistan province in Iran. Bleeding of central nervous system (CNS) is a common but life-threatening clinical presentation of severe factor XIII deficiency. The aim of this stu...

وصف كامل

التفاصيل البيبلوغرافية

الحاوية / القاعدة:	مجله دانشکده پزشکی اصفهان
المؤلفون الرئيسيون:	Majid Naderi, Akbar Dorgalaleh, Shaban Alizadeh, Ahmad Kazemi, Shadi Tabibian, Hossein Dargahi, Zahra Kashani Khatib, Meysam Kahiri, Maryamsadat Hoseini
التنسيق:	مقال
اللغة:	الفارسية
منشور في:	Isfahan University of Medical Sciences 2014-04-01
الموضوعات:	Factor XIII deficiency Central nervous system (CNS) bleeding Pro564Leu polymorphism
الوصول للمادة أونلاين:	http://jims.mui.ac.ir/index.php/jims/article/view/3299