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Fibrinogen Sumperk II MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
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