MeSH Browser

MeSH Supplementary: fibrinogen Saint-Germain I
Unique ID: C447420
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C447420
Registry Number: 0
Heading Mapped to: *Fibrinogens, Abnormal
Frequency: 2
Note: associated with dysfibrinogenemia; has heterozygous AalphaGly12Val mutation
Source: Thromb Res 2001 Aug 1;103(3):201-7
Indexing Information: Coagulation Protein Disorders
Date of Entry: 2002/02/21

fibrinogen Saint-Germain I MeSH Supplementary Concept Data 2024