MeSH Browser

MeSH Supplementary: Fibrinogen Sumperk II
Unique ID: C572668
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C572668
Entry Term(s): Fibrinogen Šumperk II
Registry Numbers: 0
Heading Mapped to: *Fibrinogens, Abnormal
Frequency: 1
Note: results in dysfibrinogenemia with two coding mutations: a heterozygous Aα Gly13Glu mutation, and a heterozygous FGA A6540T transition predicting a heterozygous Aα Ser314Cys mutation
Source: Am J Hematol. 2012 May;87(5):555-7
Date of Entry: 2012/06/12
Revision Date: 2012/06/13

Fibrinogen Sumperk II MeSH Supplementary Concept Data 2025