Sandbox GGC6: Difference between revisions

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== Disease ==
== Disease ==
Congenital afibrinogenemia (CAFBN)
Congenital afibrinogenemia (CAFBN)
This is an inherited blood disorder
This is an inherited blood disorder where the blood does not clot normally. This disease is cause by truncating mutations. Changing in position arg-35
when thrombin cleaves the site of fibrinopeptide leads to alpha- dysfibrinogenemias


== Relevance ==
== Relevance ==

Revision as of 19:08, 13 November 2020

Fibrinogen alpha chain

Caption for this structure

Drag the structure with the mouse to rotate

References