Published in
Lippincott, Williams & Wilkins, Blood Coagulation and Fibrinolysis, 2(22), p. 148-150, 2011
DOI: 10.1097/mbc.0b013e32834330d9
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A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family:
Journal article published in 2011 by
Emmanuel Levrat,
Imad Aboukhamis,
Philippe de Moerloose,
Jaafar Farho,
Sahar Chamaa,
Guido Reber,
Alexandre Fort,
Marguerite Neerman-Arbez 
This paper was not found in any repository, but could be made available legally by the author.
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