Title : Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature.

Pub. Date : 2021 Jan

PMID : 33245842






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 RESULT: Molecular analysis revealed a novel homozygous missense mutation in FGB exon 5, p.Cys241 Tyr, that was named "Fibrinogen Krakow V". Tyrosine fibrinogen beta chain Homo sapiens
2 RESULT: Molecular analysis revealed a novel homozygous missense mutation in FGB exon 5, p.Cys241 Tyr, that was named "Fibrinogen Krakow V". Tyrosine fibrinogen beta chain Homo sapiens