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Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia

(2017) Haemophilia. 23(4). p.583-589
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Chicago
Casini, A., R. Vilar, Y. Beauverd, D. Aslan, Katrien Devreese, V. Mondelaers, L. Alberio, C. Gubert, P. de Moerloose, and M. Neerman-Arbez. 2017. “Protein Modelling to Understand FGB Mutations Leading to Congenital Hypofibrinogenaemia.” Haemophilia 23 (4): 583–589.
APA
Casini, A., Vilar, R., Beauverd, Y., Aslan, D., Devreese, K., Mondelaers, V., Alberio, L., et al. (2017). Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia. Haemophilia, 23(4), 583–589.
Vancouver
1.
Casini A, Vilar R, Beauverd Y, Aslan D, Devreese K, Mondelaers V, et al. Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia. Haemophilia. Wiley; 2017;23(4):583–9.
MLA
Casini, A. et al. “Protein Modelling to Understand FGB Mutations Leading to Congenital Hypofibrinogenaemia.” Haemophilia 23.4 (2017): 583–589. Print.
@article{8612435,
  author       = {Casini, A. and Vilar, R. and Beauverd, Y. and Aslan, D. and Devreese, Katrien and Mondelaers, V. and Alberio, L. and Gubert, C. and de Moerloose, P. and Neerman-Arbez, M.},
  issn         = {1351-8216},
  journal      = {Haemophilia},
  number       = {4},
  pages        = {583--589},
  publisher    = {Wiley},
  title        = {Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia},
  url          = {http://dx.doi.org/10.1111/hae.13190},
  volume       = {23},
  year         = {2017},
}

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