A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family

Published 2011 View Full Article

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Title
A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family
Authors
Keywords
-
Journal
BLOOD COAGULATION & FIBRINOLYSIS
Volume 22, Issue 2, Pages 148-150
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2011-01-18
DOI
10.1097/mbc.0b013e32834330d9
References
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