Identification of the First Iranian Family with “γArg275Cys” Mutation (Fibrinogen Tokyo II)
| Author | Gholamreza Toogeh | en |
| Author | Maryam Helali | en |
| Author | Shaban Alizade | en |
| Author | Akbar Dorgalaleh | en |
| Issued Date | 2016-06-30 | en |
| Abstract | 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. | en |
| DOI | https://doi.org/10.22037/jcma.v1i2.11417 | en |
| Keyword | Fibrinogen | en |
| Keyword | Tokyo II | en |
| Keyword | Dysfibrinogenemia | en |
| Publisher | Brieflands | en |
| Title | Identification of the First Iranian Family with “γArg275Cys” Mutation (Fibrinogen Tokyo II) | en |
| Type | Case Report | en |
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