A novel frameshift mutation in FGA (c.1846 del A) leading...

Blood Coagulation & Fibrinolysis 2011 / 03 Vol. 22; Iss. 2

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

Levrat, Emmanuel, Aboukhamis, Imad, de Moerloose, Philippe, Farho, Jaafar, Chamaa, Sahar, Reber, Guido, Fort, Alexandre, Neerman-Arbez, Marguerite
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Volume:
22
Language:
english
Journal:
Blood Coagulation & Fibrinolysis
DOI:
10.1097/mbc.0b013e32834330d9
Date:
March, 2011
File:
PDF, 150 KB
english, 2011
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