A novel mutation in the FGB: c.1105C>T turns the codon...

Blood Cells, Molecules, and Diseases 2013 / 3 Vol. 50; Iss. 3

A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia

Marchi, Rita, Brennan, Stephen, Meyer, Michael, Rojas, Héctor, Kanzler, Daniela, De Agrela, Marisela, Ruiz-Saez, Arlette
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Volume:
50
Language:
english
Journal:
Blood Cells, Molecules, and Diseases
DOI:
10.1016/j.bcmd.2012.11.010
Date:
March, 2013
File:
PDF, 973 KB
english, 2013
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