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fibrinogen Vlissingen MeSH Supplementary Concept Data 2024


MeSH Supplementary
fibrinogen Vlissingen
Unique ID
C069866
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C069866
Registry Number
0
Heading Mapped to
*Fibrinogens, Abnormal
Frequency
3
Note
congenitally abnormal fibrinogen with a 6-base deletion in the gamma-chain gene, causing defective calcium binding & impaired fibrin polymerization
Source
J Biol Chem 1991;266(20):13456
Date of Entry
1991/08/14
Revision Date
1992/01/31
fibrinogen Vlissingen Preferred
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