Sandbox GGC6: Difference between revisions

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== Disease ==
== Disease ==
Congenital afibrinogenemia (CAFBN)
Congenital afibrinogenemia (CAFBN)
This is an inherited blood disorder where the blood does not clot normally. This disease is caused by truncating mutations. Changing in position Arg-35 when Thrombin cleaves the site of Fibrinopeptide leads to alpha- Dysfibrinogenemias.  
This is an inherited blood disorder where the blood does not clot normally. This disease is caused by truncating mutations. Changing in position Arg-35 when Thrombin cleaves the site of Fibrinopeptide leads to alpha- Dysfibrinogenemias. <ref>doi: 10.1160/TH14-07-0629</ref>





Revision as of 19:11, 13 November 2020

Fibrinogen alpha chain

Caption for this structure

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References