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 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 ==
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