Cite
HARVARD Citation
Vu, D. et al. (2005). Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the γ chain globular domain impairing fibrinogen secretion. Journal of medical genetics. 42 (9), p. e57. [Online].
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Vu, D. et al. (2005). Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the γ chain globular domain impairing fibrinogen secretion. Journal of medical genetics. 42 (9), p. e57. [Online].