MeSH Browser

MeSH Supplementary: fibrinogen Baltimore I
Unique ID: C066651
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C066651
Entry Term(s): fibrinogen St. Gallen I
Registry Number: 0
Heading Mapped to: *Fibrinogens, Abnormal
Frequency: 2
Note: congenital abnormal fibrinogen; polymerization defect associated with a gamma(292)Gly replaced by Val(GGC--GTC) mutation
Source: Blood 1990;76(11):2279
Indexing Information: Coagulation Protein Disorders
Date of Entry: 1991/01/26
Revision Date: 1999/05/27

fibrinogen Baltimore I MeSH Supplementary Concept Data 2024