Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia

Semin Thromb Hemost. 2016 Jun;42(4):455-8. doi: 10.1055/s-0036-1581104. Epub 2016 May 5.

Authors

Tomas Simurda¹, Zuzana Snahnicanova², Dusan Loderer², Juraj Sokol¹, Jan Stasko¹, Zora Lasabova², Peter Kubisz¹

Affiliations

¹ Department of Haematology and Transfusiology, Comenius University in Bratislava, Jessenius Faculty of Medicine, National Centre of Hemostasis and Thrombosis, Bratislava, Slovakia.
² Department of Molecular Biology, Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin, BioMed Martin, Slovakia.

PMID: 27148845
DOI: 10.1055/s-0036-1581104

No abstract available

Publication types

Letter

MeSH terms

Afibrinogenemia / genetics*
Codon, Nonsense*
Fibrinogens, Abnormal / genetics*
Humans

Substances

Codon, Nonsense
Fibrinogens, Abnormal