Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia
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L. Alberio | A. Casini | P. de Moerloose | M. Neerman-Arbez | V. Mondelaers | D. Aslan | K. Devreese | R. Vilar | Y. Beauverd | C. Gubert | P. D. Moerloose | Alessandro Casini | Lorenzo Alberio | Rui Vilar | Yan Beauverd