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

Published 2016 View Full Article

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Title
Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia
Authors
Keywords
-
Journal
SEMINARS IN THROMBOSIS AND HEMOSTASIS
Volume 42, Issue 04, Pages 455-458
Publisher
Georg Thieme Verlag KG
Online
2016-05-06
DOI
10.1055/s-0036-1581104

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