Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia
Journal article published in 2017 by
Alessandro Casini 
,
R. Vilar,
Y. Beauverd,
D. Aslan,
Katrien Devreese,
V. Mondelaers,
L. Alberio,
C. Gubert,
P. de Moerloose,
Marguerite Neerman-Arbez
,
R. Vilar,
Y. Beauverd,
D. Aslan,
Katrien Devreese,
V. Mondelaers,
L. Alberio,
C. Gubert,
P. de Moerloose,
Marguerite Neerman-Arbez
This paper is made freely available by the publisher.
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