Identification of the First Iranian Family with “γArg275Cys” Mutation (Fibrinogen Tokyo II)
<p>Background: Inherited fibrinogen deficiencies areclassified into two categories: quantitative, including afibrinogenemia and hypofibrinogenemia and qualitative, including dysfibrinogenemia. Any mutation in fibrinogen genes accounts for one of these disorders.</p><p>Case report:...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Shahid Beheshti University of Medical Sciences
2016-03-01
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| Series: | Journal of Cellular and Molecular Anesthesia |
| Subjects: | |
| Online Access: | http://journals.sbmu.ac.ir/jcma/article/view/11417 |