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. <ref>doi: 10.1160/TH14-07-0629</ref>
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 19:41, 13 November 2020

Fibrinogen alpha chain

Caption for this structure

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References