MeSH Browser

MeSH Supplementary: fibrinogen Vlissingen
Unique ID: C069866
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C069866
Registry Numbers: 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 MeSH Supplementary Concept Data 2025