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

Simurda, Tomas

Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia. [electronic resource] - Seminars in thrombosis and hemostasis Jun 2016 - 455-8 p. digital

Publication Type: Letter

ISSN: 1098-9064

Standard No.: 10.1055/s-0036-1581104 doi

Subjects--Topical Terms:
Afibrinogenemia--genetics
Codon, Nonsense
Fibrinogens, Abnormal--genetics
Humans

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