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factor V Stanford MeSH Supplementary Concept Data 2025


MeSH Supplementary
factor V Stanford
Unique ID
C403063
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C403063
Registry Numbers
0
Heading Mapped to
*Factor V
Frequency
1
Note
mutation caused by a 4 base insertion at NT 2856, results in a frameshift with loss of a thrombin activation site
Source
Thromb Haemost 1999 Sep;82(3):1097-9
Date of Entry
2000/01/21
Revision Date
1955/01/01
factor V Stanford Preferred
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