Sandbox GGC6: Difference between revisions

From Proteopedia
Jump to navigationJump to search
Student (talk | contribs)
No edit summary
Student (talk | contribs)
No edit summary
Line 13: Line 13:
== Disease ==
== Disease ==
Congenital afibrinogenemia (CAFBN)
Congenital afibrinogenemia (CAFBN)
  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
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. <ref>PMID: 25427968.</ref>
when thrombin cleaves the site of fibrinopeptide leads to alpha- dysfibrinogenemias.  


== Relevance ==
== Relevance ==

Revision as of 19:07, 13 November 2020

Fibrinogen alpha chain

Caption for this structure

Drag the structure with the mouse to rotate

References